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