{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2024,11,21]],"date-time":"2024-11-21T05:33:23Z","timestamp":1732167203724,"version":"3.28.0"},"reference-count":10,"publisher":"Elsevier BV","issue":"22","license":[{"start":{"date-parts":[[2024,11,1]],"date-time":"2024-11-01T00:00:00Z","timestamp":1730419200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2024,11,1]],"date-time":"2024-11-01T00:00:00Z","timestamp":1730419200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2024,9,5]],"date-time":"2024-09-05T00:00:00Z","timestamp":1725494400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"funder":[{"DOI":"10.13039\/501100001349","name":"National Medical Research Council","doi-asserted-by":"publisher","id":[{"id":"10.13039\/501100001349","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["JACC: Case Reports"],"published-print":{"date-parts":[[2024,11]]},"DOI":"10.1016\/j.jaccas.2024.102646","type":"journal-article","created":{"date-parts":[[2024,11,20]],"date-time":"2024-11-20T19:11:11Z","timestamp":1732129871000},"page":"102646","update-policy":"http:\/\/dx.doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":0,"title":["Coinheritance of Hypertrophic and Arrhythmogenic Cardiomyopathy Variants in a Patient With Hypertrophic\u00a0Cardiomyopathy"],"prefix":"10.1016","volume":"29","author":[{"given":"Yi Siang","family":"Lee","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Chee Jian","family":"Pua","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yasmin","family":"Bylstra","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Saumya","family":"Shekhar Jamuar","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Iswaree","family":"Devi Balakrishnan","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"issue":"9","key":"10.1016\/j.jaccas.2024.102646_bib1","doi-asserted-by":"crossref","first-page":"1903","DOI":"10.1016\/j.jacc.2004.07.045","article-title":"Myosin binding protein C mutations and compound heterozygosity in hypertrophic cardiomyopathy","volume":"44","author":"Van Driest","year":"2004","journal-title":"J\u00a0Am Coll Cardiol"},{"issue":"10","key":"10.1016\/j.jaccas.2024.102646_bib2","doi-asserted-by":"crossref","DOI":"10.1136\/jmg.2005.033886","article-title":"Compound and double mutations in patients with hypertrophic cardiomyopathy: implications for genetic testing and counselling","volume":"42","author":"Ingles","year":"2005","journal-title":"J\u00a0Med Genet"},{"issue":"4","key":"10.1016\/j.jaccas.2024.102646_bib3","doi-asserted-by":"crossref","DOI":"10.1161\/CIRCGENETICS.116.001666","article-title":"Multiple gene variants in hypertrophic cardiomyopathy in the era of next-generation sequencing","volume":"10","author":"Burns","year":"2017","journal-title":"Circ Cardiovasc Genet"},{"issue":"9","key":"10.1016\/j.jaccas.2024.102646_bib4","doi-asserted-by":"crossref","first-page":"485","DOI":"10.1016\/j.ejmg.2017.06.008","article-title":"Digenic inheritance of mutations in the cardiac troponin (TNNT2) and cardiac beta myosin heavy chain (MYH7) as the cause of severe dilated cardiomyopathy","volume":"60","author":"Petropoulou","year":"2017","journal-title":"Eur J Med Genet"},{"issue":"6","key":"10.1016\/j.jaccas.2024.102646_bib5","doi-asserted-by":"crossref","first-page":"1276","DOI":"10.1007\/s12265-023-10403-8","article-title":"A\u00a0systematic analysis of the clinical outcome associated with multiple reclassified desmosomal gene variants in arrhythmogenic right ventricular cardiomyopathy patients","volume":"16","author":"Nagyova","year":"2023","journal-title":"J\u00a0Cardiovasc Transl Res"},{"issue":"10","key":"10.1016\/j.jaccas.2024.102646_bib6","doi-asserted-by":"crossref","first-page":"1165","DOI":"10.1038\/ejhg.2017.109","article-title":"Co-inheritance of mutations associated with arrhythmogenic cardiomyopathy and hypertrophic cardiomyopathy","volume":"25","author":"De Bortoli","year":"2017","journal-title":"Eur J Human Genetics"},{"issue":"1","key":"10.1016\/j.jaccas.2024.102646_bib7","doi-asserted-by":"crossref","first-page":"41","DOI":"10.1016\/j.cjca.2021.08.022","article-title":"Deleterious rare desmosomal variants contribute to hypertrophic cardiomyopathy and are associated with distinctive clinical features","volume":"38","author":"Wu","year":"2022","journal-title":"Can J Cardiol"},{"issue":"6","key":"10.1016\/j.jaccas.2024.102646_bib8","doi-asserted-by":"crossref","first-page":"552","DOI":"10.1161\/CIRCGENETICS.113.000122","article-title":"Correlation of\u00a0ventricular arrhythmias with genotype in arrhythmogenic right ventricular cardiomyopathy","volume":"6","author":"Bao","year":"2013","journal-title":"Circ Cardiovasc Genet"},{"issue":"5","key":"10.1016\/j.jaccas.2024.102646_bib9","doi-asserted-by":"crossref","first-page":"281","DOI":"10.1016\/j.cardfail.2018.03.004","article-title":"Genetic evaluation of cardiomyopathy\u2014a Heart Failure Society of America practice guideline","volume":"24","author":"Hershberger","year":"2018","journal-title":"J\u00a0Card Fail"},{"issue":"6","key":"10.1016\/j.jaccas.2024.102646_bib10","doi-asserted-by":"crossref","DOI":"10.1161\/CIRCGEN.122.003704","article-title":"Prevalence and disease expression of pathogenic and likely pathogenic variants associated with inherited cardiomyopathies in the general population","volume":"15","author":"Bourfiss","year":"2022","journal-title":"Circ Genom Precis Med"}],"container-title":["JACC: Case Reports"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S2666084924006259?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S2666084924006259?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2024,11,20]],"date-time":"2024-11-20T19:11:15Z","timestamp":1732129875000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S2666084924006259"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2024,11]]},"references-count":10,"journal-issue":{"issue":"22","published-print":{"date-parts":[[2024,11]]}},"alternative-id":["S2666084924006259"],"URL":"https:\/\/doi.org\/10.1016\/j.jaccas.2024.102646","relation":{},"ISSN":["2666-0849"],"issn-type":[{"value":"2666-0849","type":"print"}],"subject":[],"published":{"date-parts":[[2024,11]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Coinheritance of Hypertrophic and Arrhythmogenic Cardiomyopathy Variants in a Patient With Hypertrophic\u00a0Cardiomyopathy","name":"articletitle","label":"Article Title"},{"value":"JACC: Case Reports","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.jaccas.2024.102646","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2024 The Authors. Published by Elsevier on behalf of the American College of Cardiology Foundation.","name":"copyright","label":"Copyright"}],"article-number":"102646"}}