Mutations in PDLIM5 are rare in dilated cardiomyopathy but are emerging as potential disease modifiers

Verdonschot, JAJ; Robinson, EL; James, KN; Mohamed, MW; Claes, GRF; Casas, K; Vanhoutte, EK; Hazebroek, MR; Kringlen, G; Pasierb, MM; van den Wijngaard, A; Glatz, JFC; Heymans, SRB; Krapels, IPC; Nahas, S; Brunner, HG; Szklarczyk, R

Verdonschot, JAJ (reprint author), MUMC, Dept Cardiol & Clin Genet, POB 5800, NL-6202 AZ Maastricht, Netherlands.

MOLECULAR GENETICS & GENOMIC MEDICINE, 0; ():

Abstract

Background A causal genetic mutation is found in 40% of families with dilated cardiomyopathy (DCM), leaving a large percentage of families genetically......

Full Text Link


Links

期刊讨论 | 中国SCI论文 | 期刊主页 | 投稿经验 | 杂志官网 | 投稿链接 | 作者需知 | PMC链接 | Pubmed全文检索