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...

Полное описание

Сохранить в:
Библиографические подробности
Главные авторы: 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
Формат: Artigo
Язык:Inglês
Опубликовано: Wiley 2020-02-01
Серии:Molecular Genetics & Genomic Medicine
Предметы:
dilated cardiomyopathy
genetic modifier
genetics
sarcomere
Online-ссылка:https://doi.org/10.1002/mgg3.1049
Метки: Добавить метку
Нет меток, Требуется 1-ая метка записи!

Схожие документы