A rare case of arrhythmogenic right ventricular cardiomyopathy associated with LAMA2 mutation: A case report and literature review


This is the first case report to describe an ARVC phenotype in patients possessing a novel LAMA2 c.8842G > A (p.G2948S) mutation. Our results aid in understanding of the pathogenesis of ARVC. The molecular mechanism of LAMA2 leading to ARVC disease still needs further study. Copyright © 2022 Wang, Fang, Zhang, Li and Luo.

Authors Wang Y, Fang Y, Zhang D, Li Y, Luo S
Journal Frontiers in medicine
Publication Date 2022;9:922347
PubMed 35924034
PubMed Central PMC9339636
DOI 10.3389/fmed.2022.922347

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