{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,1,22]],"date-time":"2026-01-22T12:30:11Z","timestamp":1769085011443,"version":"3.49.0"},"reference-count":16,"publisher":"Oxford University Press (OUP)","issue":"5","license":[{"start":{"date-parts":[[2025,12,19]],"date-time":"2025-12-19T00:00:00Z","timestamp":1766102400000},"content-version":"vor","delay-in-days":1983,"URL":"https:\/\/creativecommons.org\/licenses\/by-nc\/4.0\/"},{"start":{"date-parts":[[2020,7,15]],"date-time":"2020-07-15T00:00:00Z","timestamp":1594771200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc\/4.0\/"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":[],"published-print":{"date-parts":[[2020,10,1]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:p>We present a case of atypical LMNA cardiomyopathy associated with the pathogenic variant p.Arg541Ser. The patient had early-onset severe ventricular arrhythmias but atrioventricular conduction was normal. Segmental motion abnormalities and a large transmural scar, mainly apical and lateral, were found at cardiac magnetic resonance, corresponding to areas of severe wall thinning at computed tomography and of low voltages at electroanatomic mapping. Ventricular tachycardia ablation was successful in controlling ventricular arrhythmias. Few other cases described patients with pathogenic variants in the Arg541 residue, and they displayed similar atypical features, suggesting a genotype\u2013phenotype correlation which may have specific prognostic and therapeutic implications.<\/jats:p>","DOI":"10.1002\/ehf2.12776","type":"journal-article","created":{"date-parts":[[2020,7,15]],"date-time":"2020-07-15T08:47:00Z","timestamp":1594802820000},"page":"3169-3173","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":2,"title":["Genotype\u2013Phenotype Correlation of LMNA Variants Involving the Arg541 Residue: A Case Report with Multimodality Imaging and Literature Review"],"prefix":"10.1093","volume":"7","author":[{"given":"Andrea","family":"Di Marco*","sequence":"first","affiliation":[{"name":"Department of Cardiology, Hospital Universitari de Bellvitge , Barcelona ,","place":["Spain"]}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Mar\u00eda","family":"Ruiz-Cueto","sequence":"additional","affiliation":[{"name":"Department of Cardiology, Hospital Universitari de Bellvitge , Barcelona ,","place":["Spain"]}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Joel","family":"Salazar-Mendiguch\u00eda","sequence":"additional","affiliation":[{"name":"Department of Cardiology, Hospital Universitari de Bellvitge , Barcelona ,","place":["Spain"]}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Eduard","family":"Claver","sequence":"additional","affiliation":[{"name":"Department of Cardiology, Hospital Universitari de Bellvitge , Barcelona ,","place":["Spain"]}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Gerard","family":"Roura","sequence":"additional","affiliation":[{"name":"Department of Cardiology, Hospital Universitari de Bellvitge , Barcelona ,","place":["Spain"]}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Paolo Domenico","family":"Dallaglio","sequence":"additional","affiliation":[{"name":"Department of Cardiology, Hospital Universitari de Bellvitge , Barcelona ,","place":["Spain"]}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ignasi","family":"Anguera","sequence":"additional","affiliation":[{"name":"Department of Cardiology, Hospital Universitari de Bellvitge , Barcelona ,","place":["Spain"]}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"286","published-online":{"date-parts":[[2020,7,15]]},"reference":[{"key":"2026012114050403900_ehf212776-bib-0001","doi-asserted-by":"crossref","first-page":"33","DOI":"10.3390\/cells5030033","article-title":"Skeletal muscle laminopathies: a review of clinical and molecular 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