{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,11,2]],"date-time":"2025-11-02T12:28:45Z","timestamp":1762086525244,"version":"build-2065373602"},"reference-count":51,"publisher":"Elsevier BV","issue":"2-3","license":[{"start":{"date-parts":[[2020,6,1]],"date-time":"2020-06-01T00:00:00Z","timestamp":1590969600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2020,6,1]],"date-time":"2020-06-01T00:00:00Z","timestamp":1590969600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2021,5,29]],"date-time":"2021-05-29T00:00:00Z","timestamp":1622246400000},"content-version":"am","delay-in-days":362,"URL":"http:\/\/www.elsevier.com\/open-access\/userlicense\/1.0\/"}],"funder":[{"DOI":"10.13039\/501100004571","name":"Minist\u00c3\u00a8re des Affaires Sociales et de la Sant\u00c3\u00a9","doi-asserted-by":"publisher","id":[{"id":"10.13039\/501100004571","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["clinicalkey.com","clinicalkey.com.au","clinicalkey.es","clinicalkey.fr","clinicalkey.jp","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Annales d'Endocrinologie"],"published-print":{"date-parts":[[2020,6]]},"DOI":"10.1016\/j.ando.2020.04.007","type":"journal-article","created":{"date-parts":[[2020,4,28]],"date-time":"2020-04-28T11:20:13Z","timestamp":1588072813000},"page":"68-77","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":4,"title":["Clinical phenotype of mitochondrial diabetes due to rare mitochondrial DNA mutations"],"prefix":"10.1016","volume":"81","author":[{"given":"Anne-Ga\u00eblle","family":"Decoux-Poullot","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Sylvie","family":"Bannwarth","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Vincent","family":"Procaccio","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Anne-Sophie","family":"Lebre","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Claude","family":"Jardel","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Bernard","family":"Vialettes","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"V\u00e9ronique","family":"Paquis-Flucklinger","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Nicolas","family":"Chevalier","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"issue":"1","key":"10.1016\/j.ando.2020.04.007_bib0260","doi-asserted-by":"crossref","first-page":"51","DOI":"10.1016\/j.ando.2019.10.003","article-title":"Lipodystrophic syndromes: from diagnosis to treatment","volume":"81","author":"Sollier","year":"2020","journal-title":"Ann Endocrinol (Paris)"},{"key":"10.1016\/j.ando.2020.04.007_bib0265","article-title":"Cardiovascular complications of lipodystrophic syndromes\u00a0\u2013\u00a0focus on laminopathies","author":"Mosbah","year":"2020","journal-title":"Ann Endocrinol (Paris)"},{"issue":"8832","key":"10.1016\/j.ando.2020.04.007_bib0270","doi-asserted-by":"crossref","first-page":"1376","DOI":"10.1016\/0140-6736(92)92560-3","article-title":"Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA","volume":"340","author":"Reardon","year":"1992","journal-title":"Lancet"},{"issue":"5","key":"10.1016\/j.ando.2020.04.007_bib0275","doi-asserted-by":"crossref","first-page":"368","DOI":"10.1038\/ng0892-368","article-title":"Mutation in mitochondrial tRNA(Leu)(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness","volume":"1","author":"van den Ouweland","year":"1992","journal-title":"Nat Genet"},{"issue":"4","key":"10.1016\/j.ando.2020.04.007_bib0280","doi-asserted-by":"crossref","first-page":"375","DOI":"10.1007\/BF00400668","article-title":"Maternally inherited diabetes and deafness: a new diabetes subtype","volume":"39","author":"Maassen","year":"1996","journal-title":"Diabetologia"},{"issue":"3","key":"10.1016\/j.ando.2020.04.007_bib0285","doi-asserted-by":"crossref","first-page":"213","DOI":"10.1080\/07853890510007188","article-title":"Molecular mechanisms of mitochondrial diabetes (MIDD)","volume":"37","author":"Maassen","year":"2005","journal-title":"Ann Med"},{"issue":"2","key":"10.1016\/j.ando.2020.04.007_bib0290","doi-asserted-by":"crossref","first-page":"113","DOI":"10.2337\/diab.45.2.113","article-title":"Mitochondria and diabetes, genetic, biochemical, and clinical implications of the cellular energy circuit","volume":"45","author":"Gerbitz","year":"1996","journal-title":"Diabetes"},{"issue":"3","key":"10.1016\/j.ando.2020.04.007_bib0295","doi-asserted-by":"crossref","first-page":"216","DOI":"10.1016\/j.revmed.2008.11.017","article-title":"Diagnostic clinique et biologique du diab\u00e8te mitochondrial et particularit\u00e9s de sa prise en charge","volume":"31","author":"Meas","year":"2010","journal-title":"Rev Med Interne"},{"issue":"9 Pt 1","key":"10.1016\/j.ando.2020.04.007_bib0300","doi-asserted-by":"crossref","first-page":"721","DOI":"10.7326\/0003-4819-134-9_Part_1-200105010-00008","article-title":"Maternally inherited diabetes and deafness: a multicenter study","volume":"134","author":"Guillausseau","year":"2001","journal-title":"Ann Intern Med"},{"issue":"10","key":"10.1016\/j.ando.2020.04.007_bib0305","doi-asserted-by":"crossref","first-page":"704","DOI":"10.1136\/jmedgenet-2013-101604","article-title":"Prevalence of rare mitochondrial DNA mutations in mitochondrial disorders","volume":"50","author":"Bannwarth","year":"2013","journal-title":"J Med Genet"},{"issue":"12","key":"10.1016\/j.ando.2020.04.007_bib0310","doi-asserted-by":"crossref","first-page":"1032","DOI":"10.1002\/(SICI)1096-9136(199712)14:12<1032::AID-DIA504>3.0.CO;2-Y","article-title":"Screening of patients with maternally transmitted diabetes for mitochondrial gene mutations in the tRNA[Leu(UUR)] region","volume":"14","author":"Tsukuda","year":"1997","journal-title":"Diabet Med"},{"issue":"4","key":"10.1016\/j.ando.2020.04.007_bib0315","first-page":"271","article-title":"Diabetes mellitus and the exocrine pancreas","volume":"56","author":"Gorelick","year":"1983","journal-title":"Yale J Biol Med"},{"issue":"2","key":"10.1016\/j.ando.2020.04.007_bib0320","doi-asserted-by":"crossref","first-page":"181","DOI":"10.1016\/S1262-3636(07)70105-2","article-title":"Heterogeneity of diabetes phenotype in patients with 3243bp mutation of mitochondrial DNA (Maternally Inherited Diabetes and Deafness or MIDD)","volume":"30","author":"Guillausseau","year":"2004","journal-title":"Diabetes Metab"},{"issue":"6","key":"10.1016\/j.ando.2020.04.007_bib0325","doi-asserted-by":"crossref","first-page":"1097","DOI":"10.2337\/diacare.25.6.1097","article-title":"GAD antibody in mitochondrial diabetes associated with tRNA(UUR) mutation at position 3271","volume":"25","author":"Suzuki","year":"2002","journal-title":"Diabetes Care"},{"issue":"4 Pt 1","key":"10.1016\/j.ando.2020.04.007_bib0330","doi-asserted-by":"crossref","first-page":"386","DOI":"10.1016\/j.diabet.2008.02.002","article-title":"Auto-immune cerebellar ataxia with anti-GAD antibodies accompanied by de novo late-onset type 1 diabetes mellitus","volume":"34","author":"Bayreuther","year":"2008","journal-title":"Diabetes Metab"},{"issue":"1","key":"10.1016\/j.ando.2020.04.007_bib0335","doi-asserted-by":"crossref","first-page":"253","DOI":"10.1016\/0925-4439(95)00036-4","article-title":"Mitochondrial diabetes mellitus: a review","volume":"1271","author":"Gerbitz","year":"1995","journal-title":"Biochim Biophys Acta"},{"key":"10.1016\/j.ando.2020.04.007_bib0340","doi-asserted-by":"crossref","first-page":"151","DOI":"10.1146\/annurev.ge.29.120195.001055","article-title":"Molecular genetic aspects of human mitochondrial disorders","volume":"29","author":"Larsson","year":"1995","journal-title":"Annu Rev Genet"},{"issue":"2","key":"10.1016\/j.ando.2020.04.007_bib0345","doi-asserted-by":"crossref","first-page":"20","DOI":"10.1016\/j.metabol.2015.10.014","article-title":"Metformin-associated lactic acidosis: current perspectives on causes and risk","volume":"65","author":"DeFronzo","year":"2016","journal-title":"Metab Clin Exp"},{"issue":"8","key":"10.1016\/j.ando.2020.04.007_bib0350","doi-asserted-by":"crossref","DOI":"10.3390\/jcm6080075","article-title":"Statins, muscle disease and mitochondria","volume":"75","author":"Ramachandran","year":"2017","journal-title":"J Clin Med"},{"issue":"1","key":"10.1016\/j.ando.2020.04.007_bib0355","doi-asserted-by":"crossref","first-page":"133","DOI":"10.1097\/01.mpa.0000246659.38375.4d","article-title":"Beta-cell function in individuals carrying the mitochondrial tRNA leu (UUR) mutation","volume":"34","author":"Salles","year":"2007","journal-title":"Pancreas"},{"issue":"9","key":"10.1016\/j.ando.2020.04.007_bib0360","doi-asserted-by":"crossref","first-page":"1641","DOI":"10.1093\/clinchem\/47.9.1641","article-title":"Mitochondrial gene mutations in the tRNA(Leu(UUR)) region and diabetes: prevalence and clinical phenotypes in Japan","volume":"47","author":"Ohkubo","year":"2001","journal-title":"Clin Chem"},{"issue":"12","key":"10.1016\/j.ando.2020.04.007_bib0365","doi-asserted-by":"crossref","first-page":"2081","DOI":"10.1093\/hmg\/2.12.2081","article-title":"A new point mutation associated with mitochondrial encephalomyopathy","volume":"2","author":"Morten","year":"1993","journal-title":"Hum Mol Genet"},{"issue":"3","key":"10.1016\/j.ando.2020.04.007_bib0370","first-page":"992","article-title":"Mitochondrial deoxyribonucleic acid 3256C-T mutation in a Japanese family with noninsulin-dependent diabetes mellitus","volume":"83","author":"Hirai","year":"1998","journal-title":"J Clin Endocrinol Metab"},{"issue":"8760","key":"10.1016\/j.ando.2020.04.007_bib0375","doi-asserted-by":"crossref","first-page":"143","DOI":"10.1016\/0140-6736(91)90136-D","article-title":"Maternally inherited myopathy and cardiomyopathy: association with mutation in mitochondrial DNA tRNA(Leu)(UUR)","volume":"338","author":"Zeviani","year":"1991","journal-title":"Lancet"},{"issue":"7","key":"10.1016\/j.ando.2020.04.007_bib0380","doi-asserted-by":"crossref","first-page":"1138","DOI":"10.2337\/diacare.20.7.1138","article-title":"Diabetes associated with a novel 3264 mitochondrial tRNA(Leu)(UUR) mutation","volume":"20","author":"Suzuki","year":"1997","journal-title":"Diabetes Care"},{"issue":"11","key":"10.1016\/j.ando.2020.04.007_bib0385","doi-asserted-by":"crossref","first-page":"1304","DOI":"10.2337\/diacare.19.11.1304","article-title":"Clinical picture of a case of diabetes with mitochondrial tRNA mutation at position 3271","volume":"19","author":"Suzuki","year":"1996","journal-title":"Diabetes Care"},{"issue":"3","key":"10.1016\/j.ando.2020.04.007_bib0390","doi-asserted-by":"crossref","first-page":"952","DOI":"10.2337\/diacare.26.3.952","article-title":"Heteroplasmic mitochondrial DNA 3310 mutation in NADH dehydrogenase subunit 1 associated with type 2 diabetes, hypertrophic cardiomyopathy, and mental retardation in a single patient","volume":"26","author":"Hattori","year":"2003","journal-title":"Diabetes Care"},{"issue":"6","key":"10.1016\/j.ando.2020.04.007_bib0395","doi-asserted-by":"crossref","first-page":"318","DOI":"10.1055\/s-2005-865646","article-title":"A heteroplasmic mitochondrial DNA 3310 mutation in the ND1 gene in a patient with type 2 diabetes, hypertrophic cardiomyopathy, and mental retardation","volume":"113","author":"Hattori","year":"2005","journal-title":"Exp Clin Endocrinol Diabetes"},{"issue":"5","key":"10.1016\/j.ando.2020.04.007_bib0400","doi-asserted-by":"crossref","first-page":"625","DOI":"10.1507\/endocrj.45.625","article-title":"Mitochondrial DNA point mutation at nucleotide pair 3316 in a Japanese family with heterogeneous phenotypes of diabetes","volume":"45","author":"Nakano","year":"1998","journal-title":"Endocr J"},{"issue":"1","key":"10.1016\/j.ando.2020.04.007_bib0405","doi-asserted-by":"crossref","first-page":"147","DOI":"10.1006\/bbrc.1996.1481","article-title":"A G-to-A substitution at nucleotide position 3316 in mitochondrial DNA is associated with Japanese non-insulin-dependent diabetes mellitus","volume":"227","author":"Odawara","year":"1996","journal-title":"Biochem Biophys Res Commun"},{"issue":"1\u20132","key":"10.1016\/j.ando.2020.04.007_bib0410","doi-asserted-by":"crossref","first-page":"26","DOI":"10.1016\/j.mrfmmm.2006.07.006","article-title":"A novel mitochondrial DNA missense mutation at G3421A in a family with maternally inherited diabetes and deafness","volume":"602","author":"Chen","year":"2006","journal-title":"Mutat Res"},{"issue":"9","key":"10.1016\/j.ando.2020.04.007_bib0415","doi-asserted-by":"crossref","first-page":"1260","DOI":"10.1002\/humu.22358","article-title":"Pathogenic mitochondrial tRNA point mutations: nine novel mutations affirm their importance as a cause of mitochondrial disease","volume":"34","author":"Blakely","year":"2013","journal-title":"Hum Mutat"},{"issue":"11","key":"10.1016\/j.ando.2020.04.007_bib0420","doi-asserted-by":"crossref","first-page":"2034","DOI":"10.2337\/diacare.21.11.2034","article-title":"Impaired insulin secretion in Japanese diabetic subjects with an A-to-G mutation at nucleotide 8296 of the mitochondrial DNA in tRNA(Lys)","volume":"21","author":"Kameoka","year":"1998","journal-title":"Diabetes Care"},{"issue":"9","key":"10.1016\/j.ando.2020.04.007_bib0425","doi-asserted-by":"crossref","first-page":"2238","DOI":"10.2337\/dc07-0466","article-title":"Diabetes and deafness: is it sufficient to screen for the mitochondrial 3243A>G mutation alone?","volume":"30","author":"Whittaker","year":"2007","journal-title":"Diabetes Care"},{"issue":"12","key":"10.1016\/j.ando.2020.04.007_bib0430","doi-asserted-by":"crossref","first-page":"1428","DOI":"10.2337\/diacare.17.12.1428","article-title":"Diabetes with mitochondrial gene tRNALYS mutation","volume":"17","author":"Suzuki","year":"1994","journal-title":"Diabetes Care"},{"issue":"6","key":"10.1016\/j.ando.2020.04.007_bib0435","doi-asserted-by":"crossref","first-page":"441","DOI":"10.1007\/BF00900496","article-title":"The T-C(8356) mitochondrial DNA mutation in a Japanese family","volume":"243","author":"Sano","year":"1996","journal-title":"J Neurol"},{"issue":"3","key":"10.1016\/j.ando.2020.04.007_bib0440","doi-asserted-by":"crossref","first-page":"771","DOI":"10.1006\/bbrc.2000.3751","article-title":"variations in patients with maternally inherited diabetes and deafness syndrome","volume":"277","author":"Perucca-Lostanlen","year":"2000","journal-title":"Biochem Biophys Res Commun"},{"issue":"3","key":"10.1016\/j.ando.2020.04.007_bib0445","doi-asserted-by":"crossref","first-page":"353","DOI":"10.1016\/j.bbrc.2015.01.151","article-title":"A novel mutation MT-COIII m.9267G>C and MT-COI m.5913G>A mutation in mitochondrial genes in a Tunisian family with maternally inherited diabetes and deafness (MIDD) associated with severe nephropathy","volume":"459","author":"Tabebi","year":"2015","journal-title":"Biochem Biophys Res Commun"},{"key":"10.1016\/j.ando.2020.04.007_bib0450","doi-asserted-by":"crossref","first-page":"49","DOI":"10.1016\/j.mito.2015.01.004","article-title":"Maternally inherited diabetes is associated with a homoplasmic T10003C mutation in the mitochondrial tRNA(Gly) gene","volume":"21","author":"Liu","year":"2015","journal-title":"Mitochondrion"},{"issue":"11","key":"10.1016\/j.ando.2020.04.007_bib0455","doi-asserted-by":"crossref","first-page":"1800","DOI":"10.2337\/diabetes.47.11.1800","article-title":"Mitochondrial diabetes: investigation and identification of a novel mutation","volume":"47","author":"Lynn","year":"1998","journal-title":"Diabetes"},{"issue":"7","key":"10.1016\/j.ando.2020.04.007_bib0460","doi-asserted-by":"crossref","first-page":"2317","DOI":"10.2337\/diabetes.51.7.2317","article-title":"Defining the importance of mitochondrial gene defects in maternally inherited diabetes by sequencing the entire mitochondrial genome","volume":"51","author":"Choo-Kang","year":"2002","journal-title":"Diabetes"},{"issue":"7","key":"10.1016\/j.ando.2020.04.007_bib0465","doi-asserted-by":"crossref","first-page":"1269","DOI":"10.2337\/diabetes.49.7.1269","article-title":"A new mitochondrial DNA mutation at 14577T\/C is probably a major pathogenic mutation for maternally inherited type 2 diabetes","volume":"49","author":"Tawata","year":"2000","journal-title":"Diabetes"},{"issue":"5","key":"10.1016\/j.ando.2020.04.007_bib0470","first-page":"1017","article-title":"Segregation patterns of a novel mutation in the mitochondrial tRNA glutamic acid gene associated with myopathy and diabetes mellitus","volume":"56","author":"Hao","year":"1995","journal-title":"Am J Hum Genet"},{"issue":"11","key":"10.1016\/j.ando.2020.04.007_bib0475","doi-asserted-by":"crossref","first-page":"1731","DOI":"10.2337\/diacare.20.11.1731","article-title":"Phenotypic expression of diabetes secondary to a T14709C mutation of mitochondrial DNA. Comparison with MIDD syndrome (A3243G mutation): a case report","volume":"20","author":"Vialettes","year":"1997","journal-title":"Diabetes Care"},{"issue":"4","key":"10.1016\/j.ando.2020.04.007_bib0480","doi-asserted-by":"crossref","first-page":"270","DOI":"10.1016\/j.jdiacomp.2009.11.002","article-title":"The heteroplasmic m.14709T>C mutation in the tRNA(Glu) gene in two Tunisian families with mitochondrial diabetes","volume":"24","author":"Mezghani","year":"2010","journal-title":"J Diabetes Complicat"},{"issue":"2","key":"10.1016\/j.ando.2020.04.007_bib0485","doi-asserted-by":"crossref","first-page":"207","DOI":"10.1515\/JPEM.1999.12.2.207","article-title":"Early onset of diabetes mellitus associated with the mitochondrial DNA T14709C point mutation: patient report and literature review","volume":"12","author":"Damore","year":"1999","journal-title":"J Pediatr Endocrinol Metab"},{"issue":"5","key":"10.1016\/j.ando.2020.04.007_bib0490","first-page":"1026","article-title":"Congenital encephalomyopathy and adult-onset myopathy and diabetes mellitus: different phenotypic associations of a new heteroplasmic mtDNA tRNA glutamic acid mutation","volume":"56","author":"Hanna","year":"1995","journal-title":"Am J Hum Genet"},{"issue":"4","key":"10.1016\/j.ando.2020.04.007_bib0495","doi-asserted-by":"crossref","first-page":"334","DOI":"10.1046\/j.1464-5491.2001.00429-2.x","article-title":"Association of the T14709C mutation of mitochondrial DNA with maternally inherited diabetes mellitus and\/or deafness in an Italian family","volume":"18","author":"Rigoli","year":"2001","journal-title":"Diabet Med"},{"issue":"2","key":"10.1016\/j.ando.2020.04.007_bib0500","doi-asserted-by":"crossref","first-page":"80","DOI":"10.1055\/s-2004-815754","article-title":"A novel 7301-bp deletion in mitochondrial DNA in a patient with Kearns-Sayre syndrome, diabetes mellitus, and primary amenorrhoea","volume":"112","author":"De Block","year":"2004","journal-title":"Exp Clin Endocrinol Diabetes"},{"issue":"1","key":"10.1016\/j.ando.2020.04.007_bib0505","doi-asserted-by":"crossref","first-page":"100","DOI":"10.1016\/S0002-9394(99)80243-8","article-title":"Macular dystrophy, diabetes, and deafness associated with a large mitochondrial DNA deletion","volume":"125","author":"Souied","year":"1998","journal-title":"Am J Ophthalmol"},{"issue":"1","key":"10.1016\/j.ando.2020.04.007_bib0510","doi-asserted-by":"crossref","first-page":"11","DOI":"10.1038\/ng0492-11","article-title":"Maternally transmitted diabetes and deafness associated with a 10.4kb mitochondrial DNA deletion","volume":"1","author":"Ballinger","year":"1992","journal-title":"Nat Genet"}],"container-title":["Annales d'Endocrinologie"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0003426620300640?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0003426620300640?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,11,2]],"date-time":"2025-11-02T12:25:14Z","timestamp":1762086314000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0003426620300640"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2020,6]]},"references-count":51,"journal-issue":{"issue":"2-3","published-print":{"date-parts":[[2020,6]]}},"alternative-id":["S0003426620300640"],"URL":"https:\/\/doi.org\/10.1016\/j.ando.2020.04.007","relation":{},"ISSN":["0003-4266"],"issn-type":[{"type":"print","value":"0003-4266"}],"subject":[],"published":{"date-parts":[[2020,6]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Clinical phenotype of mitochondrial diabetes due to rare mitochondrial DNA mutations","name":"articletitle","label":"Article Title"},{"value":"Annales d'Endocrinologie","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.ando.2020.04.007","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2020 Elsevier Masson SAS. All rights reserved.","name":"copyright","label":"Copyright"}]}}