{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,19]],"date-time":"2026-03-19T21:49:27Z","timestamp":1773956967793,"version":"3.50.1"},"reference-count":6,"publisher":"Elsevier BV","issue":"3","license":[{"start":{"date-parts":[[2020,3,1]],"date-time":"2020-03-01T00:00:00Z","timestamp":1583020800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2020,3,1]],"date-time":"2020-03-01T00:00:00Z","timestamp":1583020800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2019,12,18]],"date-time":"2019-12-18T00:00:00Z","timestamp":1576627200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"content-domain":{"domain":["jacc.org","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["JACC: Case Reports"],"published-print":{"date-parts":[[2020,3]]},"DOI":"10.1016\/j.jaccas.2019.11.075","type":"journal-article","created":{"date-parts":[[2020,2,26]],"date-time":"2020-02-26T14:01:21Z","timestamp":1582725681000},"page":"372-377","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":6,"title":["Novel FHL1 Mutation Associated With Hypertrophic Cardiomyopathy, Sudden\u00a0Cardiac Death, and Myopathy"],"prefix":"10.1016","volume":"2","author":[{"given":"M. Scott","family":"Binder","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Emily","family":"Brown","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Thomas","family":"Aversano","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Kathryn R.","family":"Wagner","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hugh","family":"Calkins","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Andreas S.","family":"Barth","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.jaccas.2019.11.075_bib1","doi-asserted-by":"crossref","first-page":"237","DOI":"10.1016\/j.nmd.2011.01.001","article-title":"Four and a half LIM protein 1 gene mutations cause four distinct human myopathies: a comprehensive review of the clinical, histological and pathological features","volume":"21","author":"Cowling","year":"2011","journal-title":"Neuromuscul Disord"},{"key":"10.1016\/j.jaccas.2019.11.075_bib2","doi-asserted-by":"crossref","first-page":"3681","DOI":"10.2174\/138161209789271861","article-title":"It takes two to tango: the structure and function of LIM, RING, PHD and MYND domains","volume":"15","author":"Matthews","year":"2009","journal-title":"Curr Pharm Des"},{"key":"10.1016\/j.jaccas.2019.11.075_bib3","doi-asserted-by":"crossref","first-page":"171","DOI":"10.1111\/cge.12760","article-title":"Unclassifiable arrhythmic cardiomyopathy associated with Emery-Dreifuss caused by a mutation in FHL1","volume":"90","author":"San Rom\u00e1n","year":"2016","journal-title":"Clin Genet"},{"key":"10.1016\/j.jaccas.2019.11.075_bib4","doi-asserted-by":"crossref","first-page":"1211","DOI":"10.1177\/0883073814549807","article-title":"X-linked recessive distal myopathy with hypertrophic cardiomyopathy caused by a novel mutation in the FHL1 gene","volume":"30","author":"D\u2019Arcy","year":"2015","journal-title":"J\u00a0Child Neurol"},{"key":"10.1016\/j.jaccas.2019.11.075_bib5","doi-asserted-by":"crossref","first-page":"e91","DOI":"10.1016\/j.jacc.2017.10.054","article-title":"2017 AHA\/ACC\/HRS guideline for management of patients with ventricular arrhythmias and the prevention of sudden cardiac death","volume":"72","author":"Al-Khatib","year":"2018","journal-title":"J\u00a0Am Coll Cardiol"},{"key":"10.1016\/j.jaccas.2019.11.075_bib6","first-page":"364","article-title":"Hypertrophic cardiomyopathy: clinical update","volume":"6","author":"Geske","year":"2018","journal-title":"J\u00a0Am Coll Cardiol HF"}],"container-title":["JACC: Case Reports"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S2666084919306692?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S2666084919306692?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,11,12]],"date-time":"2025-11-12T18:46:39Z","timestamp":1762973199000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S2666084919306692"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2020,3]]},"references-count":6,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2020,3]]}},"alternative-id":["S2666084919306692"],"URL":"https:\/\/doi.org\/10.1016\/j.jaccas.2019.11.075","relation":{},"ISSN":["2666-0849"],"issn-type":[{"value":"2666-0849","type":"print"}],"subject":[],"published":{"date-parts":[[2020,3]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Novel FHL1 Mutation Associated With Hypertrophic Cardiomyopathy, Sudden\u00a0Cardiac Death, and Myopathy","name":"articletitle","label":"Article Title"},{"value":"JACC: Case Reports","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.jaccas.2019.11.075","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2020 The Authors. Published by Elsevier on behalf of the American College of Cardiology Foundation.","name":"copyright","label":"Copyright"}]}}