{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,9,25]],"date-time":"2025-09-25T00:20:28Z","timestamp":1758759628952,"version":"3.44.0"},"reference-count":10,"publisher":"Elsevier BV","license":[{"start":{"date-parts":[[2024,3,1]],"date-time":"2024-03-01T00:00:00Z","timestamp":1709251200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2024,3,1]],"date-time":"2024-03-01T00:00:00Z","timestamp":1709251200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"}],"funder":[{"DOI":"10.13039\/501100004479","name":"Natural Science Foundation of Jiangxi Province","doi-asserted-by":"publisher","award":["20202BAB216010"],"award-info":[{"award-number":["20202BAB216010"]}],"id":[{"id":"10.13039\/501100004479","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["clinicalkey.com","clinicalkey.com.au","clinicalkey.es","clinicalkey.fr","clinicalkey.jp","thrombosisresearch.com","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Thrombosis Research"],"published-print":{"date-parts":[[2024,3]]},"DOI":"10.1016\/j.thromres.2024.02.006","type":"journal-article","created":{"date-parts":[[2024,2,6]],"date-time":"2024-02-06T12:55:36Z","timestamp":1707224136000},"page":"122-124","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":1,"special_numbering":"C","title":["Frequency of the p.Thr241Asn mutation in Chinese patients with congenital factor VII deficiency"],"prefix":"10.1016","volume":"235","author":[{"given":"Puhui","family":"Zhou","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yan","family":"Peng","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Qingcheng","family":"Li","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Qingshui","family":"Huang","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yunyuan","family":"Kong","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"issue":"2","key":"10.1016\/j.thromres.2024.02.006_bb0005","doi-asserted-by":"crossref","first-page":"102","DOI":"10.1097\/MBC.0b013e328343641a","article-title":"Recurrent mutations and genotype-phenotype correlations in hereditary factor VII deficiency in Korea","volume":"22","author":"Kwon","year":"2011","journal-title":"Blood Coagul. Fibrinolysis"},{"issue":"4","key":"10.1016\/j.thromres.2024.02.006_bb0010","doi-asserted-by":"crossref","first-page":"327","DOI":"10.1007\/s004390000373","article-title":"Molecular analysis of the genotype-phenotype relationship in factor VII deficiency","volume":"107","author":"Millar","year":"2000","journal-title":"Hum. Genet."},{"issue":"2","key":"10.1016\/j.thromres.2024.02.006_bb0015","first-page":"124","article-title":"Novel double heterozygous mutations on Met306Val and Thr181Asn related to a hereditary coagulation factor VII deficiency","volume":"86","author":"Tu","year":"2006","journal-title":"Zhonghua Yi Xue Za Zhi"},{"issue":"1","key":"10.1016\/j.thromres.2024.02.006_bb0020","doi-asserted-by":"crossref","first-page":"143","DOI":"10.1111\/j.1365-2141.2000.02332.x","article-title":"Two novel factor VII gene mutations in a Chinese family with factor VII deficiency","volume":"111","author":"Au","year":"2000","journal-title":"Br. J. Haematol."},{"issue":"3","key":"10.1016\/j.thromres.2024.02.006_bb0025","doi-asserted-by":"crossref","first-page":"829","DOI":"10.3324\/haematol.2019.217539","article-title":"Next-generation sequencing and recombinant expression characterized aberrant splicing mechanisms and provided correction strategies in factor VII deficiency","volume":"105","author":"Ferraresi","year":"2020","journal-title":"Haematologica"},{"issue":"8","key":"10.1016\/j.thromres.2024.02.006_bb0030","doi-asserted-by":"crossref","first-page":"1455","DOI":"10.1160\/TH17-02-0085","article-title":"F7 gene variants modulate protein levels in a large cohort of patients with factor VII deficiency. Results from a genotype-phenotype study","volume":"117","author":"Quintavalle","year":"2017","journal-title":"Thromb. Haemost."},{"issue":"4","key":"10.1016\/j.thromres.2024.02.006_bb0035","doi-asserted-by":"crossref","first-page":"393","DOI":"10.1055\/s-2000-8458","article-title":"Molecular biology and clinical manifestation of hereditary factor VII deficiency","volume":"26","author":"Herrmann","year":"2000","journal-title":"Semin. Thromb. Hemost."},{"issue":"10","key":"10.1016\/j.thromres.2024.02.006_bb0040","doi-asserted-by":"crossref","first-page":"1774","DOI":"10.1111\/j.1538-7836.2004.00921.x","article-title":"Characterization of mutations causing factor VII deficiency in 61 unrelated Israeli patients","volume":"2","author":"Fromovich-Amit","year":"2004","journal-title":"J. Thromb. Haemost."},{"issue":"5","key":"10.1016\/j.thromres.2024.02.006_bb0045","doi-asserted-by":"crossref","first-page":"446","DOI":"10.1007\/BF00216448","article-title":"Molecular analysis of factor VII deficiency in Italy: a frequent mutation (FVII Lazio) in a repeated intronic region","volume":"92","author":"Bernardi","year":"1993","journal-title":"Hum. Genet."},{"issue":"6","key":"10.1016\/j.thromres.2024.02.006_bb0050","doi-asserted-by":"crossref","first-page":"489","DOI":"10.1002\/1098-1004(200006)15:6<489::AID-HUMU1>3.0.CO;2-J","article-title":"Twenty two novel mutations of the factor VII gene in factor VII deficiency","volume":"15","author":"Wulff","year":"2000","journal-title":"Hum. Mutat."}],"container-title":["Thrombosis Research"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0049384824000410?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0049384824000410?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,9,24]],"date-time":"2025-09-24T17:53:10Z","timestamp":1758736390000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0049384824000410"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2024,3]]},"references-count":10,"alternative-id":["S0049384824000410"],"URL":"https:\/\/doi.org\/10.1016\/j.thromres.2024.02.006","relation":{},"ISSN":["0049-3848"],"issn-type":[{"type":"print","value":"0049-3848"}],"subject":[],"published":{"date-parts":[[2024,3]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Frequency of the p.Thr241Asn mutation in Chinese patients with congenital factor VII deficiency","name":"articletitle","label":"Article Title"},{"value":"Thrombosis Research","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.thromres.2024.02.006","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"simple-article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2024 Elsevier Ltd. All rights reserved.","name":"copyright","label":"Copyright"}]}}