{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,1,27]],"date-time":"2026-01-27T10:36:29Z","timestamp":1769510189593,"version":"3.49.0"},"reference-count":48,"publisher":"Elsevier BV","license":[{"start":{"date-parts":[[2015,6,1]],"date-time":"2015-06-01T00:00:00Z","timestamp":1433116800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2015,2,24]],"date-time":"2015-02-24T00:00:00Z","timestamp":1424736000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"content-domain":{"domain":["ijcha-journal.com","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["IJC Heart & Vasculature"],"published-print":{"date-parts":[[2015,6]]},"DOI":"10.1016\/j.ijcha.2015.02.008","type":"journal-article","created":{"date-parts":[[2015,3,1]],"date-time":"2015-03-01T00:31:54Z","timestamp":1425169914000},"page":"99-105","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":3,"special_numbering":"C","title":["Novel linkage of LMNA Single Nucleotide Polymorphism with Dilated Cardiomyopathy in an Indian case study"],"prefix":"10.1016","volume":"7","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-5321-8658","authenticated-orcid":false,"given":"Avinanda","family":"Banerjee","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Pradip K.","family":"Ghoshal","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Kaushik","family":"Sengupta","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"issue":"23","key":"10.1016\/j.ijcha.2015.02.008_bb0005","doi-asserted-by":"crossref","first-page":"1564","DOI":"10.1056\/NEJM199412083312307","article-title":"Idiopathic dilated cardiomyopathy","volume":"331","author":"Dec","year":"1994","journal-title":"N Eng J Med"},{"issue":"14","key":"10.1016\/j.ijcha.2015.02.008_bb0010","doi-asserted-by":"crossref","first-page":"1807","DOI":"10.1161\/CIRCULATIONAHA.106.174287","volume":"113","author":"Maron","year":"2006","journal-title":"Circulation"},{"issue":"8","key":"10.1016\/j.ijcha.2015.02.008_bb0015","doi-asserted-by":"crossref","first-page":"919","DOI":"10.1111\/j.1540-8167.2006.00530.x","article-title":"Dilated cardiomyopathy: a tale of cytoskeletal proteins and beyond","volume":"17","author":"Towbin","year":"2006","journal-title":"J Cardiovasc Electrophysiol"},{"issue":"1","key":"10.1016\/j.ijcha.2015.02.008_bb0020","doi-asserted-by":"crossref","first-page":"27","DOI":"10.1186\/1750-1172-1-27","article-title":"Cardiomyopathy, familial dilated","volume":"1","author":"Taylor","year":"2006","journal-title":"Orphanet J Rare Dis"},{"issue":"16","key":"10.1016\/j.ijcha.2015.02.008_bb0025","doi-asserted-by":"crossref","first-page":"1641","DOI":"10.1016\/j.jacc.2011.01.015","article-title":"Update 2011: clinical and genetic issues in familial dilated cardiomyopathy","volume":"57","author":"Hershberger","year":"2011","journal-title":"J Am Coll Cardiol"},{"issue":"5","key":"10.1016\/j.ijcha.2015.02.008_bb0030","doi-asserted-by":"crossref","first-page":"771","DOI":"10.1016\/S0735-1097(02)02954-6","article-title":"Natural history of dilated cardiomyopathy due to lamin A\/C gene mutations","volume":"41","author":"Taylor","year":"2003","journal-title":"J Am Coll Cardiol"},{"issue":"3","key":"10.1016\/j.ijcha.2015.02.008_bb0035","doi-asserted-by":"crossref","first-page":"180","DOI":"10.1054\/jcaf.2003.24","article-title":"Care processes and clinical outcomes of continuous outpatient support with inotropes (COSI) in patients with refractory endstage heart failure","volume":"9","author":"Hershberger","year":"2003","journal-title":"J Card Fail"},{"issue":"3","key":"10.1016\/j.ijcha.2015.02.008_bb0040","doi-asserted-by":"crossref","first-page":"249","DOI":"10.1054\/jcaf.2001.26339","article-title":"Novel lamin A\/C mutations in two families with dilated cardiomyopathy and conduction system disease","volume":"7","author":"Jakobs","year":"2001","journal-title":"J Card Fail"},{"issue":"1","key":"10.1016\/j.ijcha.2015.02.008_bb0045","doi-asserted-by":"crossref","first-page":"90","DOI":"10.1007\/s00395-008-0748-6","article-title":"Identification of mutational hot spots in LMNA encoding lamin A\/C in patients with familial dilated cardiomyopathy","volume":"104","author":"Perrot","year":"2009","journal-title":"Basic Res Cardiol"},{"issue":"6","key":"10.1016\/j.ijcha.2015.02.008_bb0050","doi-asserted-by":"crossref","first-page":"981","DOI":"10.1016\/S0735-1097(02)01724-2","article-title":"Autosomal dominant dilated cardiomyopathy with atrioventricular block: a lamin A\/C defect-related disease","volume":"39","author":"Arbustini","year":"2002","journal-title":"J Am Coll Cardiol"},{"issue":"15","key":"10.1016\/j.ijcha.2015.02.008_bb0055","doi-asserted-by":"crossref","first-page":"1250","DOI":"10.1016\/j.jacc.2008.06.044","article-title":"Long-term outcome and risk stratification in dilated cardiolaminopathies","volume":"52","author":"Pasotti","year":"2008","journal-title":"J Am Coll Cardiol"},{"issue":"8","key":"10.1016\/j.ijcha.2015.02.008_bb0060","doi-asserted-by":"crossref","first-page":"560","DOI":"10.1136\/jmg.40.8.560","article-title":"Expanding the phenotype of LMNA mutations in dilated cardiomyopathy and functional consequences of these mutations","volume":"40","author":"Sebillon","year":"2003","journal-title":"J Med Genet"},{"issue":"6","key":"10.1016\/j.ijcha.2015.02.008_bb0065","doi-asserted-by":"crossref","first-page":"628","DOI":"10.1093\/eurjhf\/hft013","article-title":"Genetic analysis in 418 index patients with idiopathic dilated cardiomyopathy: overview of 10years' experience","volume":"15","author":"KY","year":"2013","journal-title":"Eur J Heart Fail"},{"issue":"10","key":"10.1016\/j.ijcha.2015.02.008_bb0070","doi-asserted-by":"crossref","first-page":"2041","DOI":"10.1016\/j.jacc.2004.08.028","article-title":"Genetics of dilated cardiomyopathy: more genes that kill","volume":"44","author":"Towbin","year":"2004","journal-title":"J Am Coll Cardiol"},{"issue":"23","key":"10.1016\/j.ijcha.2015.02.008_bb0075","doi-asserted-by":"crossref","first-page":"1715","DOI":"10.1056\/NEJM199912023412302","article-title":"Missense mutations in the rod domain of the lamin A\/C gene as causes of dilated cardiomyopathy and conduction-system disease","volume":"341","author":"Fatkin","year":"1999","journal-title":"New Eng J Med"},{"issue":"22","key":"10.1016\/j.ijcha.2015.02.008_bb0080","doi-asserted-by":"crossref","first-page":"16321","DOI":"10.1016\/S0021-9258(19)85424-8","article-title":"Structural organization of the human gene encoding nuclear lamin A and nuclear lamin C","volume":"268","author":"Lin","year":"1993","journal-title":"J Biol Chem"},{"issue":"11","key":"10.1016\/j.ijcha.2015.02.008_bb0085","doi-asserted-by":"crossref","first-page":"848","DOI":"10.1038\/nrm950","article-title":"Lamins: building blocks or regulators of gene expression?","volume":"3","author":"Hutchison","year":"2002","journal-title":"Nat Rev Mol Cell Biol"},{"issue":"5","key":"10.1016\/j.ijcha.2015.02.008_bb0090","doi-asserted-by":"crossref","first-page":"553","DOI":"10.1097\/00019052-200410000-00005","article-title":"Laminopathies: from the heart of the cell to the clinics","volume":"17","author":"Benedetti","year":"2004","journal-title":"Curr Opin Neurol"},{"issue":"1","key":"10.1016\/j.ijcha.2015.02.008_bb0095","doi-asserted-by":"crossref","first-page":"257","DOI":"10.1042\/BST0380257","article-title":"Genotype\u2013phenotype correlations in laminopathies: how does fate translate?","volume":"38","author":"Scharner","year":"2010","journal-title":"Biochem Soc Trans"},{"issue":"1","key":"10.1016\/j.ijcha.2015.02.008_bb0100","doi-asserted-by":"crossref","first-page":"39","DOI":"10.1152\/physiolgenomics.2000.3.1.39","article-title":"Genetic variation in LMNA modulates plasma leptin and indices of obesity in aboriginal Canadians","volume":"3","author":"Hegele","year":"2000","journal-title":"Physiol Genomics"},{"issue":"6","key":"10.1016\/j.ijcha.2015.02.008_bb0105","first-page":"2747","article-title":"Common genomic variation in LMNA modulates indexes of obesity in Inuit 1","volume":"86","author":"Hegele","year":"2001","journal-title":"J Clin Endocrinol Metabol"},{"issue":"3","key":"10.1016\/j.ijcha.2015.02.008_bb0110","doi-asserted-by":"crossref","first-page":"231","DOI":"10.1006\/mgme.2001.3147","article-title":"Subcutaneous abdominal adipocyte size, a predictor of type 2 diabetes, is linked to chromosome 1q21\u2013q23 and is associated with a common polymorphism in LMNA in pima Indians","volume":"72","author":"Weyer","year":"2001","journal-title":"Mol Genet Metab"},{"issue":"1","key":"10.1016\/j.ijcha.2015.02.008_bb0115","doi-asserted-by":"crossref","first-page":"79","DOI":"10.1007\/s00109-004-0589-1","article-title":"Meta-analysis of clinical characteristics of 299 carriers of LMNA gene mutations: do lamin A\/C mutations portend a high risk of sudden death?","volume":"83","author":"van Berlo","year":"2005","journal-title":"J Mol Med"},{"issue":"5","key":"10.1016\/j.ijcha.2015.02.008_bb0120","doi-asserted-by":"crossref","first-page":"841","DOI":"10.1161\/01.CIR.93.5.841","article-title":"Report of the 1995 World Health Organization\/International Society and Federation of Cardiology Task Force on the definition and classification of car diomyopathies","volume":"93","author":"Richardson","year":"1996","journal-title":"Circulation"},{"issue":"9","key":"10.1016\/j.ijcha.2015.02.008_bb0125","doi-asserted-by":"crossref","first-page":"892","DOI":"10.1016\/j.clinbiochem.2009.01.016","article-title":"Validation of high-resolution DNA melting analysis for mutation scanning of the LMNA gene","volume":"42","author":"Millat","year":"2009","journal-title":"Clin Biochem"},{"issue":"9","key":"10.1016\/j.ijcha.2015.02.008_bb0130","doi-asserted-by":"crossref","first-page":"1065","DOI":"10.1093\/eurheartj\/ehr105","article-title":"A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy","volume":"32","author":"Villard","year":"2011","journal-title":"Eur Heart J"},{"issue":"5","key":"10.1016\/j.ijcha.2015.02.008_bb0135","doi-asserted-by":"crossref","first-page":"642","DOI":"10.1111\/j.1365-2265.2011.04111.x","article-title":"Genotype of the LMNA 1908C> T variant is associated with generalized obesity in Asian Indians in North India","volume":"75","author":"Sharma","year":"2011","journal-title":"Clin Endocrinol"},{"issue":"7","key":"10.1016\/j.ijcha.2015.02.008_bb0140","doi-asserted-by":"crossref","first-page":"288","DOI":"10.4103\/0019-5359.55114","article-title":"Epidemiology and genetics of dilated cardiomyopathy in the Indian context","volume":"63","author":"Ushasree","year":"2009","journal-title":"Indian J Med Sci"},{"issue":"12","key":"10.1016\/j.ijcha.2015.02.008_bb0145","doi-asserted-by":"crossref","first-page":"6699","DOI":"10.1210\/jc.2005-0939","article-title":"Phenotypic heterogeneity in body fat distribution in patients with atypical Werner's syndrome due to heterozygous Arg133Leu lamin A\/C mutation","volume":"90","author":"Jacob","year":"2005","journal-title":"J Clin Endocrinol Metabol"},{"issue":"5","key":"10.1016\/j.ijcha.2015.02.008_bb0150","doi-asserted-by":"crossref","first-page":"590","DOI":"10.1111\/j.1469-1809.2008.00456.x","article-title":"Founder effect and estimation of the age of the c. 892C> T (p. Arg298Cys) mutation in LMNA associated to Charcot\u2013Marie\u2013Tooth subtype CMT2B1 in families from North Western Africa","volume":"72","author":"Hamadouche","year":"2008","journal-title":"Ann Hum Genet"},{"issue":"9","key":"10.1016\/j.ijcha.2015.02.008_bb0155","doi-asserted-by":"crossref","first-page":"1563","DOI":"10.1016\/j.neurobiolaging.2008.08.020","article-title":"Polymorphisms in LMNA and near a SERPINA gene cluster are associated with cognitive function in older people","volume":"31","author":"Cluett","year":"2010","journal-title":"Neurobiol Aging"},{"issue":"1","key":"10.1016\/j.ijcha.2015.02.008_bb0160","doi-asserted-by":"crossref","first-page":"32","DOI":"10.1016\/j.neulet.2011.08.051","article-title":"Polymorphisms in LMNA and near a SERPINA13 gene are not associated with cognitive performance in Chinese elderly males without dementia","volume":"504","author":"Yeh","year":"2011","journal-title":"Neurosci Lett"},{"issue":"8","key":"10.1016\/j.ijcha.2015.02.008_bb0165","first-page":"637","article-title":"[Disorders of laminins in diseases of myocardial and skeletal muscles]","volume":"49","author":"Spinarova","year":"2003","journal-title":"Vnitr Lek"},{"issue":"9","key":"10.1016\/j.ijcha.2015.02.008_bb0170","doi-asserted-by":"crossref","first-page":"1708","DOI":"10.1161\/01.ATV.0000136384.53705.c9","article-title":"Variation in the Lamin A\/C gene associations with metabolic syndrome","volume":"24","author":"Steinle","year":"2004","journal-title":"Arterioscler Thromb Vasc Biol"},{"issue":"8","key":"10.1016\/j.ijcha.2015.02.008_bb0175","doi-asserted-by":"crossref","first-page":"3884","DOI":"10.1210\/jc.2009-2675","article-title":"LMNA rs4641 and the muscle lamin A and C isoforms in twins\u2014Metabolic implications and transcriptional regulation","volume":"95","author":"Wegner","year":"2010","journal-title":"J Clin Endocrinol Metabol"},{"issue":"3","key":"10.1016\/j.ijcha.2015.02.008_bb0180","doi-asserted-by":"crossref","first-page":"694","DOI":"10.2337\/db06-0927","article-title":"Common variation in LMNA increases susceptibility to type 2 diabetes and associates with elevated fasting glycemia and estimates of body fat and height in the general population studies of 7,495 Danish Whites","volume":"56","author":"Wegner","year":"2007","journal-title":"Diabetes"},{"issue":"3","key":"10.1016\/j.ijcha.2015.02.008_bb0185","doi-asserted-by":"crossref","first-page":"884","DOI":"10.2337\/db06-1055","article-title":"Lamin A\/C polymorphisms, type 2 diabetes, and the metabolic syndrome case\u2013control and quantitative trait studies","volume":"56","author":"Mesa","year":"2007","journal-title":"Diabetes"},{"issue":"1","key":"10.1016\/j.ijcha.2015.02.008_bb0190","doi-asserted-by":"crossref","first-page":"76","DOI":"10.1007\/s00125-007-0857-z","article-title":"Evaluating the association of common LMNA variants with type 2 diabetes and quantitative metabolic phenotypes in French Europids","volume":"51","author":"Duesing","year":"2008","journal-title":"Diabetologia"},{"issue":"19","key":"10.1016\/j.ijcha.2015.02.008_bb0195","doi-asserted-by":"crossref","first-page":"1916","DOI":"10.1016\/j.jacc.2012.05.059","article-title":"Quantitative expression of the mutated lamin A\/C gene in patients with cardiolaminopathy","volume":"60","author":"Narula","year":"2012","journal-title":"J Am Coll Cardiol"},{"issue":"3","key":"10.1016\/j.ijcha.2015.02.008_bb0200","doi-asserted-by":"crossref","first-page":"285","DOI":"10.1038\/6799","article-title":"Mutations in the gene encoding lamin A\/C cause autosomal dominant Emery\u2013Dreifuss muscular dystrophy","volume":"21","author":"Bonne","year":"1999","journal-title":"Nat Genet"},{"issue":"3","key":"10.1016\/j.ijcha.2015.02.008_bb0205","doi-asserted-by":"crossref","first-page":"726","DOI":"10.1086\/339274","article-title":"Homozygous defects in LMNA, encoding lamin A\/C nuclear-envelope proteins, cause autosomal recessive axonal neuropathy in human (Charcot\u2013Marie\u2013Tooth disorder type 2) and mouse","volume":"70","author":"De Sandre-Giovannoli","year":"2002","journal-title":"Am J Hum Genet"},{"issue":"1","key":"10.1016\/j.ijcha.2015.02.008_bb0210","doi-asserted-by":"crossref","first-page":"109","DOI":"10.1093\/hmg\/9.1.109","article-title":"Nuclear lamin A\/C R482Q mutation in Canadian kindreds with Dunnigan-type familial partial lipodystrophy","volume":"9","author":"Cao","year":"2000","journal-title":"Hum Mol Genet"},{"issue":"2","key":"10.1016\/j.ijcha.2015.02.008_bb0215","doi-asserted-by":"crossref","first-page":"153","DOI":"10.1038\/72807","article-title":"LMNA, encoding lamin A\/C, is mutated in partial lipodystrophy","volume":"24","author":"Shackleton","year":"2000","journal-title":"Nat Genet"},{"issue":"6","key":"10.1016\/j.ijcha.2015.02.008_bb0220","doi-asserted-by":"crossref","first-page":"660","DOI":"10.1161\/CIRCRESAHA.113.300282","article-title":"Genetic cardiomyopathies causing heart failure","volume":"113","author":"Cahill","year":"2013","journal-title":"Circ Res"},{"issue":"2","key":"10.1016\/j.ijcha.2015.02.008_bb0225","doi-asserted-by":"crossref","first-page":"158","DOI":"10.1016\/j.jmoldx.2012.09.002","article-title":"Inherited cardiomyopathies: molecular genetics and clinical genetic testing in the postgenomic era","volume":"15","author":"Teekakirikul","year":"2013","journal-title":"J Mol Diagn"},{"issue":"8","key":"10.1016\/j.ijcha.2015.02.008_bb0230","doi-asserted-by":"crossref","first-page":"1077","DOI":"10.1093\/europace\/eur245","article-title":"HRS\/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA)","volume":"13","author":"Ackerman","year":"2011","journal-title":"Europace"},{"issue":"7","key":"10.1016\/j.ijcha.2015.02.008_bb0235","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1007\/s11886-013-0375-1","article-title":"Genetic evaluation of dilated cardiomyopathy","volume":"15","author":"Morales","year":"2013","journal-title":"Curr Cardiol Rep"},{"issue":"10","key":"10.1016\/j.ijcha.2015.02.008_bb0240","doi-asserted-by":"crossref","first-page":"e78104","DOI":"10.1371\/journal.pone.0078104","article-title":"Whole exome sequencing identifies a troponin T mutation hot spot in familial dilated cardiomyopathy","volume":"8","author":"Campbell","year":"2013","journal-title":"PLoS One"}],"container-title":["IJC Heart & Vasculature"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S235290671500024X?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S235290671500024X?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2022,5,1]],"date-time":"2022-05-01T02:52:59Z","timestamp":1651373579000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S235290671500024X"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2015,6]]},"references-count":48,"alternative-id":["S235290671500024X"],"URL":"https:\/\/doi.org\/10.1016\/j.ijcha.2015.02.008","relation":{},"ISSN":["2352-9067"],"issn-type":[{"value":"2352-9067","type":"print"}],"subject":[],"published":{"date-parts":[[2015,6]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Novel linkage of LMNA Single Nucleotide Polymorphism with Dilated Cardiomyopathy in an Indian case study","name":"articletitle","label":"Article Title"},{"value":"IJC Heart & Vasculature","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.ijcha.2015.02.008","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"Copyright \u00a9 2015 Published by Elsevier Ireland Ltd.","name":"copyright","label":"Copyright"}]}}