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

Abstract Background A causal genetic mutation is found in 40% of families with dilated cardiomyopathy (DCM), leaving a large percentage of families genetically unsolved. This prevents adequate counseling and clear recommendations in these families. We aim to identify novel genes or modifiers associa...

全面介紹

Na minha lista:
書目詳細資料
Main Authors: Job A. J. Verdonschot, Emma L. Robinson, Kiely N. James, Mohamed W. Mohamed, Godelieve R. F. Claes, Kari Casas, Els K. Vanhoutte, Mark R. Hazebroek, Gabriel Kringlen, Michele M. Pasierb, Arthur van denWijngaard, Jan F. C. Glatz, Stephane R. B. Heymans, Ingrid P. C. Krapels, Shareef Nahas, Han G. Brunner, Radek Szklarczyk
格式: Artigo
語言:Inglês
出版: Wiley 2020-02-01
叢編:Molecular Genetics & Genomic Medicine
主題:
dilated cardiomyopathy
genetic modifier
genetics
sarcomere
在線閱讀:https://doi.org/10.1002/mgg3.1049
標簽: 添加標簽
沒有標簽, 成為第一個標記此記錄!

相似書籍