{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,11,1]],"date-time":"2025-11-01T05:11:41Z","timestamp":1761973901193,"version":"build-2065373602"},"reference-count":6,"publisher":"Elsevier BV","issue":"4","license":[{"start":{"date-parts":[[2024,4,1]],"date-time":"2024-04-01T00:00:00Z","timestamp":1711929600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2024,4,1]],"date-time":"2024-04-01T00:00:00Z","timestamp":1711929600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2025,4,1]],"date-time":"2025-04-01T00:00:00Z","timestamp":1743465600000},"content-version":"vor","delay-in-days":365,"URL":"http:\/\/www.elsevier.com\/open-access\/userlicense\/1.0\/"}],"funder":[{"DOI":"10.13039\/100000050","name":"NHLBI","doi-asserted-by":"publisher","id":[{"id":"10.13039\/100000050","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["clinicalkey.com","clinicalkey.com.au","clinicalkey.es","clinicalkey.fr","clinicalkey.jp","jacc.org","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["JACC: Heart Failure"],"published-print":{"date-parts":[[2024,4]]},"DOI":"10.1016\/j.jchf.2023.11.014","type":"journal-article","created":{"date-parts":[[2024,1,10]],"date-time":"2024-01-10T13:58:21Z","timestamp":1704895101000},"page":"754-756","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":0,"title":["Monoallelic TTN Truncation Variants Identified in Individuals With DCM May\u00a0Cause a Mild Skeletal Myopathy"],"prefix":"10.1016","volume":"12","author":[{"given":"J. Travis","family":"Hinson","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ray E.","family":"Hershberger","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.jchf.2023.11.014_bib1","doi-asserted-by":"crossref","unstructured":"Skriver SV, Krett B, Poulsen NS, et\u00a0al. Skeletal muscle involvement in patients with truncations of titin and familial dilated cardiomyopathy. J Am Coll Cardiol HF. 2024;12(4):740-753.","DOI":"10.1016\/j.jchf.2023.10.010"},{"key":"10.1016\/j.jchf.2023.11.014_bib2","doi-asserted-by":"crossref","first-page":"1065","DOI":"10.1161\/hh2301.100981","article-title":"The complete gene sequence of titin, expression of an unusual approximately 700-kDa titin isoform, and its interaction with obscurin identify a novel Z-line to I-band linking system","volume":"89","author":"Bang","year":"2001","journal-title":"Circ Res"},{"key":"10.1016\/j.jchf.2023.11.014_bib3","doi-asserted-by":"crossref","first-page":"59","DOI":"10.1161\/01.RES.86.1.59","article-title":"Differential expression of cardiac titin isoforms and modulation of cellular stiffness","volume":"86","author":"Cazorla","year":"2000","journal-title":"Circ Res"},{"key":"10.1016\/j.jchf.2023.11.014_bib4","first-page":"293","article-title":"Increasing role of titin mutations in neuromuscular disorders","volume":"3","author":"Savarese","year":"2016","journal-title":"J\u00a0Neuromuscul Dis"},{"key":"10.1016\/j.jchf.2023.11.014_bib5","doi-asserted-by":"crossref","first-page":"46","DOI":"10.1038\/ng.3719","article-title":"Titin-truncating variants affect heart function\u00a0in disease cohorts and the general\u00a0population","volume":"49","author":"Schafer","year":"2017","journal-title":"Nat Genet"},{"key":"10.1016\/j.jchf.2023.11.014_bib6","doi-asserted-by":"crossref","DOI":"10.1126\/scitranslmed.abd7287","article-title":"Truncated titin proteins in dilated cardiomyopathy","volume":"13","author":"McAfee","year":"2021","journal-title":"Sci Transl Med"}],"container-title":["JACC: Heart Failure"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S2213177923007783?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S2213177923007783?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,11,1]],"date-time":"2025-11-01T05:04:06Z","timestamp":1761973446000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S2213177923007783"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2024,4]]},"references-count":6,"journal-issue":{"issue":"4","published-print":{"date-parts":[[2024,4]]}},"alternative-id":["S2213177923007783"],"URL":"https:\/\/doi.org\/10.1016\/j.jchf.2023.11.014","relation":{},"ISSN":["2213-1779"],"issn-type":[{"type":"print","value":"2213-1779"}],"subject":[],"published":{"date-parts":[[2024,4]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Monoallelic TTN Truncation Variants Identified in Individuals With DCM May\u00a0Cause a Mild Skeletal Myopathy","name":"articletitle","label":"Article Title"},{"value":"JACC: Heart Failure","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.jchf.2023.11.014","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"https:\/\/doi.org\/10.1016\/j.jchf.2023.10.010","name":"associatedlink","label":"CrossRef DOI link to the associated document"},{"value":"simple-article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2024 by the American College of Cardiology Foundation. Published by Elsevier.","name":"copyright","label":"Copyright"}]}}