{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,18]],"date-time":"2026-09-18T10:46:08Z","timestamp":1789728368845,"version":"4.0.1"},"reference-count":42,"publisher":"Springer Science and Business Media LLC","issue":"1","license":[{"start":{"date-parts":[[2024,1,25]],"date-time":"2024-01-25T00:00:00Z","timestamp":1706140800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.springernature.com\/gp\/researchers\/text-and-data-mining"},{"start":{"date-parts":[[2024,1,25]],"date-time":"2024-01-25T00:00:00Z","timestamp":1706140800000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/www.springernature.com\/gp\/researchers\/text-and-data-mining"}],"content-domain":{"domain":["link.springer.com"],"crossmark-restriction":false},"short-container-title":["Mol Biol Rep"],"published-print":{"date-parts":[[2024,12]]},"DOI":"10.1007\/s11033-023-09027-7","type":"journal-article","created":{"date-parts":[[2024,1,25]],"date-time":"2024-01-25T17:15:42Z","timestamp":1706202942000},"update-policy":"https:\/\/doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":3,"title":["ATR1 A1166C (rs5186), FII G20210A (rs1799963), FV G1691A (rs6025), FXIII 97G\u2009>\u2009T (rs11466016) and MTHFR A1298C (rs1801131) polymorphisms and the risk of ST-elevation myocardial infarction in young Mexican individuals"],"prefix":"10.1007","volume":"51","author":[{"given":"Irma","family":"Isordia-Salas","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"David","family":"Santiago-Germ\u00e1n","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Rosa Mar\u00eda","family":"Jim\u00e9nez-Alvarado","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Reyes Ismael","family":"Carrillo-Ju\u00e1rez","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Alfredo","family":"Lea\u00f1os-Miranda","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"297","published-online":{"date-parts":[[2024,1,25]]},"reference":[{"key":"9027_CR1","doi-asserted-by":"publisher","first-page":"136","DOI":"10.1016\/j.mayocp.2019.05.001","volume":"95","author":"R Gulati","year":"2020","unstructured":"Gulati R, Behfar A, Narula J, Kanwar A, Lerman A, Cooper L, Singh M (2020) Acute Myocardial Infarction in Young individuals. Mayo Clin Proc 95:136\u2013156","journal-title":"Mayo Clin Proc"},{"key":"9027_CR2","doi-asserted-by":"publisher","first-page":"361","DOI":"10.3892\/br.2016.717","volume":"5","author":"W Hmimech","year":"2016","unstructured":"Hmimech W, Idrissi HH, Diakite B, Baghdadi D, Korchi F, Habbal R, Nadifi S (2016) Association of C677T MTHFR and G20210A FII prothrombin polymorphism with susceptibility to Myocardial Infarction. Biomed Rep 5:361\u2013366","journal-title":"Biomed Rep"},{"key":"9027_CR3","doi-asserted-by":"publisher","first-page":"653","DOI":"10.1007\/s10528-016-9744-y","volume":"54","author":"A Kallel","year":"2016","unstructured":"Kallel A, Sba\u00ef MH, S\u00e9diri Y, Feki M, Mourali MS, Mechmeche R, Jemaa R, Kaabachi N (2016) Association between the G20210A polymorphism of Prothrombin Gene and Myocardial Infarction in Tunisian Population. Biochem Genet 54:653\u2013664","journal-title":"Biochem Genet"},{"key":"9027_CR4","doi-asserted-by":"publisher","first-page":"100048","DOI":"10.1016\/j.rpth.2023.100048","volume":"11","author":"P Agosti","year":"2023","unstructured":"Agosti P, Mancini I, Sadeghian S, Pagliari MT, Abbasi SH, Pourhosseini H, Boroumand M, Lotfi-Tokaldany M, Pappalardo E, Maino A, Rosendaal FR, Peyvandi F (2023) Factor V Leiden but not the factor II 20210G\u2009>\u2009A mutation is a risk factor for premature coronary artery Disease: a case-control study in Iran. Res Pract Thromb Haemost Jan 11:7:100048. https:\/\/doi.org\/10.1016\/j.rpth.2023.100048","journal-title":"Res Pract Thromb Haemost Jan"},{"key":"9027_CR5","doi-asserted-by":"publisher","first-page":"237","DOI":"10.3349\/ymj.2008.49.2.237","volume":"49","author":"B Ercan","year":"2008","unstructured":"Ercan B, Tamer L, Sucu N, Pekdemir H, Camsari A, Atik U (2008) Factor V Leiden and prothrombin G20210A gene polymorphisms in patients with coronary artery Disease. Yonsei Med J 49:237\u2013243","journal-title":"Yonsei Med J"},{"key":"9027_CR6","doi-asserted-by":"publisher","first-page":"346","DOI":"10.1016\/j.clinbiochem.2013.12.006","volume":"47","author":"M Boroumand","year":"2014","unstructured":"Boroumand M, Pourgholi L, Ziaee S, Anvari MS, Jalali A, Goodarzynejad H (2014) The association between Factor V Leiden with the presence and severity of coronary artery Disease. Clin Biochem 47:346\u2013360","journal-title":"Clin Biochem"},{"key":"9027_CR7","doi-asserted-by":"publisher","first-page":"535","DOI":"10.1177\/1076029615572466","volume":"22","author":"W Alkhiary","year":"2016","unstructured":"Alkhiary W, Azzam H, Yossof MM, Aref S, Othman M, El-Sharawy S (2016) Association of hemostatic gene polymorphisms with early-onset Ischemic Heart Disease in Egyptian patients. Clin Appl Thromb Hemost 22:535\u2013542","journal-title":"Clin Appl Thromb Hemost"},{"issue":"1","key":"9027_CR8","doi-asserted-by":"publisher","first-page":"1857525","DOI":"10.1080\/19932820.2020.1857525","volume":"16","author":"A Msalati","year":"2021","unstructured":"Msalati A, Bashein A, Ghrew M, Sedaa K, Ali A, Zaid A (2021) Association of venous thromboembolism and Myocardial Infarction with factor V Leiden and factor II gene mutations among Libyan patients. Libyan J Med 16(1):1857525. https:\/\/doi.org\/10.1080\/19932820.2020.1857525","journal-title":"Libyan J Med"},{"key":"9027_CR9","doi-asserted-by":"publisher","first-page":"2235","DOI":"10.1007\/s11033-008-9439-5","volume":"36","author":"A Var","year":"2009","unstructured":"Var A, Ut\u00fck O, Ak\u00e7ali S, Sanlida\u011f T, Uyanik BS, Din\u00e7 G (2009) Impact of hemostatic gene single point mutations in patients with non-diabetic coronary artery Disease. Mol Biol Rep 36:2235\u20132243","journal-title":"Mol Biol Rep"},{"key":"9027_CR10","doi-asserted-by":"publisher","first-page":"74","DOI":"10.5603\/CJ.a2016.0070","volume":"24","author":"JH Jung","year":"2017","unstructured":"Jung JH, Song GG, Kim JH, Seo YH, Choi SJ (2017) Association of factor XIII Val34Leu polymorphism and coronary artery Disease: a meta-analysis. Cardiol J 24:74\u201384","journal-title":"Cardiol J"},{"key":"9027_CR11","first-page":"5547","volume":"7","author":"G Wang","year":"2014","unstructured":"Wang G, Zou Z, Ji X, Ni Q, Ma Z (2014) Factor XIII-A Val34Leu polymorphism might be associated with Myocardial Infarction risk: an updated meta-analysis. Int J Clin Exp Med 7:5547\u20135552","journal-title":"Int J Clin Exp Med"},{"key":"9027_CR12","doi-asserted-by":"publisher","first-page":"519","DOI":"10.1007\/s11239-019-01856-3","volume":"48","author":"M Ambroziak","year":"2019","unstructured":"Ambroziak M, Kury\u0142owicz A, Budaj AJ (2019) Increased coagulation factor XIII activity but not genetic variants of coagulation factors is associated with Myocardial Infarction in young patients. Thromb Thrombolysis 48:519\u2013527","journal-title":"Thromb Thrombolysis"},{"key":"9027_CR13","doi-asserted-by":"publisher","first-page":"307","DOI":"10.1177\/1470320312466927","volume":"15","author":"X Feng","year":"2014","unstructured":"Feng X, Bao-Shi Zheng J-J, Shi J, Qian W, He H-F, Zhou (2014) A systematic review and meta-analysis of the association between angiotensin II type 1 receptor A1166C gene polymorphism and Myocardial Infarction susceptibility. Renin Angiotensin Aldosterone Syst 15:307\u2013315","journal-title":"Renin Angiotensin Aldosterone Syst"},{"key":"9027_CR14","doi-asserted-by":"publisher","first-page":"595","DOI":"10.1177\/1470320310391833","volume":"12","author":"S Mehri","year":"2011","unstructured":"Mehri S, Mahjoub S, Finsterer J, Zaroui A, Mechmeche R, Baudin B, Hammami M (2011) The CC genotype of the angiotensin II type I receptor gene independently associates with acute Myocardial Infarction in a Tunisian population. Renin Angiotensin Aldosterone Syst 12:595\u2013600","journal-title":"Renin Angiotensin Aldosterone Syst"},{"key":"9027_CR15","doi-asserted-by":"publisher","first-page":"727","DOI":"10.1007\/s40200-022-01041-z","volume":"21","author":"MT Abdul-Hasan","year":"2022","unstructured":"Abdul-Hasan MT, Omara AM, Al-Koofee DAF (2022) Association amongst human A1166C polymorphism of the angiotensin II type 1 receptor gene with coronary artery Disease in the Iraqi population. J Diabetes Metab Disord 21:727\u2013733","journal-title":"J Diabetes Metab Disord"},{"key":"9027_CR16","first-page":"189","volume":"53","author":"C Eftychiou","year":"2012","unstructured":"Eftychiou C, Antoniades L, Makri L, Koumas L, Costeas PA, Kyriakou E, Nicolaides E, Papadogiannis D (2012) Homocysteine levels and MTHFR polymorphisms in young patients with acute Myocardial Infarction: a case control study. Hellenic J Cardiol 53:189\u2013194","journal-title":"Hellenic J Cardiol"},{"key":"9027_CR17","doi-asserted-by":"publisher","first-page":"541","DOI":"10.1186\/s13104-020-05367-w","volume":"13","author":"AM Mohammad","year":"2020","unstructured":"Mohammad AM, Othman GO, Saeed CH, Al Allawi S, Gedeon GS, Qadir SM, Al-Allawi N (2020) Genetic polymorphisms in early-onset Myocardial Infarction in a sample of Iraqi patients: a pilot study. BMC Res Notes 13:541","journal-title":"BMC Res Notes"},{"key":"9027_CR18","first-page":"1371","volume":"13","author":"MC Badescu","year":"2023","unstructured":"Badescu MC, Butnariu LI, Costache AD, Gheorghe L, Seritean Isac PN, Chetran A, Leanc\u0103 SA, Afr\u0103s\u00e2nie I, Duca \u0218T, Gorduza EV, Costache II, Rezus C (2023) Acute Myocardial Infarction in patients with Hereditary Thrombophilia-A Focus on Factor V Leiden and Prothrombin G20210A. Life (Basel) 13:1371","journal-title":"Life (Basel)"},{"key":"9027_CR19","doi-asserted-by":"publisher","first-page":"212","DOI":"10.1016\/j.gene.2017.10.043","volume":"641","author":"AAA El-Fattah","year":"2018","unstructured":"El-Fattah AAA, Sadik NAH, Sedrak H, Battah A, Nabil M (2018) Association of genetic variants of hemostatic genes with myocardial infarctionin Egyptian patients. Gene 641:212\u2013219","journal-title":"Gene"},{"key":"9027_CR20","doi-asserted-by":"publisher","first-page":"267","DOI":"10.1007\/s11239-017-1520-2","volume":"44","author":"LS Rallidis","year":"2017","unstructured":"Rallidis LS, Gialeraki A, Tsirebolos G, Tsalavoutas S, Rallidi M, Iliodromitis E (2017) Prothrombotic genetic risk factors in patients with very early ST-segment elevation Myocardial Infarction. Thromb Thrombolysis 44:267\u2013273","journal-title":"Thromb Thrombolysis"},{"key":"9027_CR21","doi-asserted-by":"publisher","first-page":"13550","DOI":"10.1038\/s41598-017-13623-6","volume":"7","author":"C Li","year":"2017","unstructured":"Li C, Ren H, Chen H, Song J, Li S, Lee C, Liu J, Cui Y (2017) Prothrombin G20210A (rs1799963) polymorphism increases Myocardial Infarction risk in an age-related manner: a systematic review and meta-analysis. Sci Rep 7:13550. https:\/\/doi.org\/10.1038\/s41598-017-13623-6","journal-title":"Sci Rep"},{"key":"9027_CR22","doi-asserted-by":"publisher","first-page":"39","DOI":"10.1016\/j.carpath.2012.03.002","volume":"22","author":"DB Ben Slama","year":"2013","unstructured":"Ben Slama DB, Fekih-Mrissa N, Haggui A, Nsiri B, Baraket N, Haouala H, Gritli N (2013) Lack of association between factor V Leiden and prothrombin G20210A polymorphisms in Tunisian subjects with a history of Myocardial Infarction. Cardiovasc Pathol 22:39\u201341","journal-title":"Cardiovasc Pathol"},{"key":"9027_CR23","doi-asserted-by":"publisher","first-page":"252","DOI":"10.1097\/MBC.0b013e3283255487","volume":"20","author":"Z Rahimi","year":"2009","unstructured":"Rahimi Z, Nomani H, Mozafari H, Vaisi-Raygani A, Madani H, Malek-Khosravi S, Parsian A (2009) Factor V G1691A, prothrombin G20210A and methylenetetrahydrofolate reductase polymorphism C677T are not associated with coronary artery Disease and type 2 Diabetes Mellitus in western Iran. Blood Coagul Fibrinolysis 20:252\u2013256","journal-title":"Blood Coagul Fibrinolysis"},{"issue":"11","key":"9027_CR24","doi-asserted-by":"publisher","first-page":"e020025","DOI":"10.1161\/JAHA.120.020025","volume":"10","author":"BK Mahmoodi","year":"2021","unstructured":"Mahmoodi BK, Eriksson N, Vos GJA, Meijer K, Siegbahn A, James S, Wallentin L, Ten Berg JM (2021) Factor V Leiden does not modify the phenotype of Acute Coronary Syndrome or the extent of myocardial necrosis. J Am Heart Assoc 10(11):e020025. https:\/\/doi.org\/10.1161\/JAHA.120.020025","journal-title":"J Am Heart Assoc"},{"key":"9027_CR25","doi-asserted-by":"publisher","first-page":"1085","DOI":"10.1160\/TH07-12-0755","volume":"99","author":"LS Rallidis","year":"2008","unstructured":"Rallidis LS, Politou M, Komporozos C, Panagiotakos DB, Belessi Ch I, Travlou A, Lekakis J, Kremastinos DT (2008) Factor XIII Val34Leu polymorphism and the risk of Myocardial Infarction under the age of 36 years. Thromb Haemost 99:1085\u20131089","journal-title":"Thromb Haemost"},{"key":"9027_CR26","doi-asserted-by":"publisher","first-page":"1","DOI":"10.15517\/rbt.v54i1.13978","volume":"54","author":"L Salazar-S\u00e1nchez","year":"2006","unstructured":"Salazar-S\u00e1nchez L, Chaves L, Mayra Cartin M, Schuster G, Wulff K, Schr\u00f6der W, Herrmann FH (2006) Common polymorphisms and cardiovascular factors in patients with Myocardial Infarction of Costa Rica. Rev Biol Trop 54:1\u201311","journal-title":"Rev Biol Trop"},{"key":"9027_CR27","doi-asserted-by":"publisher","first-page":"3454","DOI":"10.3390\/jcm11123454","volume":"11","author":"B Sarecka-Hujar","year":"2022","unstructured":"Sarecka-Hujar B, \u0141oboda D, Paradowska-Nowakowska E, Go\u0142ba KS (2022) Coagulation factor XIII Val34Leu polymorphism in the prediction of premature Cardiovascular events-the results of two Meta-analyses. J Clin Med 11:3454","journal-title":"J Clin Med"},{"key":"9027_CR28","doi-asserted-by":"publisher","first-page":"519","DOI":"10.1007\/s11239-019-01856-3","volume":"48","author":"M Ambroziak","year":"2019","unstructured":"Ambroziak M, Kury\u0142owicz A, Budaj A (2019) Increased coagulation factor XIII activity but not genetic variants of coagulation factors is associated with Myocardial Infarction in young patients. J Thromb Thrombolysis 48:519\u2013527","journal-title":"J Thromb Thrombolysis"},{"key":"9027_CR29","doi-asserted-by":"publisher","first-page":"181","DOI":"10.1177\/1470320312447652","volume":"14","author":"K Zhang","year":"2013","unstructured":"Zhang K, Zhang K, Zhou B, Zhang L (2013) Association study of angiotensin II type 1 receptor: A1166C (rs5186) polymorphism with coronary Heart Disease using systematic meta-analysis. J Renin Angiotensin Aldosterone Syst 14:181\u2013188. https:\/\/doi.org\/10.1177\/1470320312447652","journal-title":"J Renin Angiotensin Aldosterone Syst"},{"key":"9027_CR30","doi-asserted-by":"publisher","first-page":"156","DOI":"10.1016\/j.carpath.2010.04.002","volume":"20","author":"MM Morales-Suarez-Varela","year":"2011","unstructured":"Morales-Suarez-Varela MM, Riera-Fortuny C, Mansego ML, Martinez-Triguero ML, Chaves FJ, Martin-Moreno JM, Ba\u00f1uls C, Hernandez-Mijares A (2011) Association between AT C573T polymorphism and cardiovascular risk factors in Myocardial Infarction. Cardiovasc Pathol 20:3:156\u2013161","journal-title":"Cardiovasc Pathol"},{"key":"9027_CR31","doi-asserted-by":"publisher","first-page":"1258","DOI":"10.1111\/j.1538-7836.2011.04273.x","volume":"9","author":"H Zhang","year":"2011","unstructured":"Zhang H, Sun ML, Peng J, Sun T, Zhang Y, Yang JM (2011) Association of the angiotensin type 1 receptor gene A1166C polymorphismswith Myocardial Infarction: a meta-analysis. J Thromb Haemost 9:1258\u20131260","journal-title":"J Thromb Haemost"},{"key":"9027_CR32","doi-asserted-by":"publisher","first-page":"190","DOI":"10.1536\/ihj.13-288","volume":"55","author":"M Hara","year":"2014","unstructured":"Hara M, Sakata Y, Nakatani D, Suna S, Usami M, Matsumoto S, Sugitani T, Ozaki K, Nishino M, Sato H, Kitamura T, Nanto S, Hamasaki T, Tanaka T, Hori M, Komuro I, OACIS Investigators (2014) Renin-angiotensin-aldosterone system polymorphisms and 5-year mortality in survivors of acute Myocardial Infarction: a report from the Osaka Acute Coronary Insufficiency Study. Int Heart J 55:190\u2013196","journal-title":"Int Heart J"},{"key":"9027_CR33","doi-asserted-by":"publisher","first-page":"174","DOI":"10.1177\/1470320309342758","volume":"10","author":"KV Karunakar","year":"2009","unstructured":"Bhoomi Reddy Pullareddy, Baddela Muni Venkata Srikanth Babu, Karunakar KV, Yasovanthi J, Potham Sampath Kumar J, Sharath PS, Jyothy A A (2009) Angiotensin II type 1 receptor gene polymorphism in Myocardial Infarction patients. J Renin Angiotensin Aldosterone Syst 10:174\u2013178","journal-title":"J Renin Angiotensin Aldosterone Syst"},{"key":"9027_CR34","doi-asserted-by":"publisher","first-page":"224","DOI":"10.1007\/s12291-021-00982-1","volume":"37","author":"RR Shivkar","year":"2022","unstructured":"Shivkar RR, Gawade GC, Padwal MK, Diwan AG, Mahajan SA, Kadam Ch Y (2022) Association of MTHFR C677T (rs1801133) and A1298C (rs1801131) polymorphisms with serum homocysteine, folate and vitamin B12 in patients with Young Coronary Artery Disease. Indian J Clin Biochem 37:224\u2013231","journal-title":"Indian J Clin Biochem"},{"key":"9027_CR35","doi-asserted-by":"publisher","first-page":"99","DOI":"10.1016\/j.ijcard.2016.04.181","volume":"217","author":"S Alizadeh","year":"2016","unstructured":"Alizadeh S, Djafarian K, Moradi S, Shab-Bidar S (2016) C667T and A1298C polymorphisms of methylenetetrahydrofolate reductase gene and susceptibility to Myocardial Infarction: a systematic review and meta-analysis. Int J Cardiol 217:99\u2013108","journal-title":"Int J Cardiol"},{"key":"9027_CR36","doi-asserted-by":"crossref","unstructured":"Irma Isordia-Salas 1, Alfredo Lea\u00f1os-Miranda, Gabriela Borrayo-S\u00e1nchez (2010) the Glu298ASP polymorphism of the endothelial nitric oxide synthase gene is associated with premature ST elevation Myocardial Infarction in Mexican population. Clin Chim Acta 411:553\u2013557","DOI":"10.1016\/j.cca.2010.01.013"},{"key":"9027_CR37","doi-asserted-by":"publisher","first-page":"163","DOI":"10.1007\/s11010-013-1794-4","volume":"384","author":"BE Rivera-Garc\u00eda","year":"2013","unstructured":"Rivera-Garc\u00eda BE, Esparza-Garc\u00eda JC, Aceves-Chimal JL, Lea\u00f1os-Miranda A, Majluf-Cruz A, Isordia-Salas I (2013) Platelet glycoprotein IIIA PIA1\/A2 polymorphism in young patients with ST elevation Myocardial Infarction and idiopathic ischemic Stroke. Mol Cell Biochem 384:163\u2013171","journal-title":"Mol Cell Biochem"},{"key":"9027_CR38","doi-asserted-by":"publisher","first-page":"3745735","DOI":"10.1155\/2019\/3745735","volume":"2019","author":"I Isordia-Salas","year":"2019","unstructured":"Isordia-Salas I, Mart\u00ednez-Marino M, Alberti-Minutti P, Ricardo-Moreno MT, Castro-Calvo R, Santiago-Germ\u00e1n D, Alvarado-Moreno JA, Calleja-Carre\u00f1o C, Hern\u00e1ndez-Ju\u00e1rez J, Lea\u00f1os-Miranda A, Majluf-Cruz A (2019) Genetic polymorphisms Associated with thrombotic Disease comparison of two territories: Myocardial Infarction and ischemic Stroke. Dis Markers 2019:3745735. https:\/\/doi.org\/10.1155\/2019\/3745735","journal-title":"Dis Markers"},{"key":"9027_CR39","doi-asserted-by":"publisher","first-page":"267","DOI":"10.1097\/MBC.0000000000000714","volume":"29","author":"I Isordia-Salas","year":"2018","unstructured":"Isordia-Salas I, Alvarado-Moreno JA, Jim\u00e9nez-Alvarado RM, Hern\u00e1ndez-Ju\u00e1rez J, Santiago-Germ\u00e1n D, Lea\u00f1os-Miranda A, Majluf-Cruz A (2018) Association of renin-angiotensin system genes polymorphisms and risk of premature ST elevation Myocardial Infarction in young Mexican population. Blood Coagul Fibrinolysis 29:267\u2013274","journal-title":"Blood Coagul Fibrinolysis"},{"key":"9027_CR40","doi-asserted-by":"publisher","first-page":"365","DOI":"10.1016\/S0300-8932(09)70893-0","volume":"62","author":"I Isordia-Salas","year":"2009","unstructured":"Isordia-Salas I, Lea\u00f1os-Miranda A, Sainz IM, Reyes-Maldonado E, Borrayo-S\u00e1nchez G (2009) Association of the plasminogen activator inhibitor-1 gene 4G\/5G polymorphism with ST elevation acute Myocardial Infarction in young patients. Rev Esp Cardiol 62:365\u2013363","journal-title":"Rev Esp Cardiol"},{"key":"9027_CR41","doi-asserted-by":"publisher","first-page":"246","DOI":"10.1016\/j.arcmed.2010.04.008","volume":"41","author":"I Isordia-Salas","year":"2010","unstructured":"Isordia-Salas I, Trejo-Aguilar A, Valad\u00e9s-Mej\u00eda MG, Santiago-Germ\u00e1n D, Lea\u00f1os-Miranda A, Mendoza-Vald\u00e9z L, J\u00e1uregui-Aguilar R, Borrayo-S\u00e1nchez G, Majluf-Cruz A (2010) C677T polymorphism of the 5,10 MTHFR gene in young Mexican subjects with ST-elevation Myocardial Infarction. Arch Med Res 41:246\u2013250","journal-title":"Arch Med Res"},{"key":"9027_CR42","first-page":"595","volume":"82","author":"MG Valades-Mej\u00eda","year":"2014","unstructured":"Valades-Mej\u00eda MG, Dom\u00ednguez-L\u00f3pez ML, Aceves-Chimal JL, Miranda AL, Majluf-Cruz A, Isordia-Salas I (2014) Study of the polymorphism R353Q in the coagulation factor VII gene and the N700S in the thrombospondin-1 gene in young patients with acute Myocardial Infarction. Cir Cir 82:595\u2013606","journal-title":"Cir Cir"}],"container-title":["Molecular Biology Reports"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/link.springer.com\/content\/pdf\/10.1007\/s11033-023-09027-7.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/link.springer.com\/article\/10.1007\/s11033-023-09027-7\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/link.springer.com\/content\/pdf\/10.1007\/s11033-023-09027-7.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2025,2,4]],"date-time":"2025-02-04T21:01:58Z","timestamp":1738702918000},"score":1,"resource":{"primary":{"URL":"https:\/\/link.springer.com\/10.1007\/s11033-023-09027-7"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2024,1,25]]},"references-count":42,"journal-issue":{"issue":"1","published-print":{"date-parts":[[2024,12]]}},"alternative-id":["9027"],"URL":"https:\/\/doi.org\/10.1007\/s11033-023-09027-7","relation":{},"ISSN":["0301-4851","1573-4978"],"issn-type":[{"value":"0301-4851","type":"print"},{"value":"1573-4978","type":"electronic"}],"subject":[],"published":{"date-parts":[[2024,1,25]]},"assertion":[{"value":"18 July 2023","order":1,"name":"received","label":"Received","group":{"name":"ArticleHistory","label":"Article History"}},{"value":"14 November 2023","order":2,"name":"accepted","label":"Accepted","group":{"name":"ArticleHistory","label":"Article History"}},{"value":"25 January 2024","order":3,"name":"first_online","label":"First Online","group":{"name":"ArticleHistory","label":"Article History"}},{"order":1,"name":"Ethics","group":{"name":"EthicsHeading","label":"Declarations"}},{"value":"The study protocol was approved by the Human Ethical Committee, and Medical Research Council of the Instituto Mexicano del Seguro Social, and conforms to the ethical guidelines of the 1975 Declaration of Helsinki. Protocol number. R-2011-3609-24.","order":2,"name":"Ethics","group":{"name":"EthicsHeading","label":"Ethical statement"}},{"value":"No conflicts of interest.","order":3,"name":"Ethics","group":{"name":"EthicsHeading","label":"Conflicts of interest"}},{"value":"The authors declare no competing interests.","order":4,"name":"Ethics","group":{"name":"EthicsHeading","label":"Competing interests"}}],"article-number":"208"}}