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...

पूर्ण विवरण

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ग्रंथसूची विवरण
मुख्य लेखकों: 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
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: Wiley 2020-02-01
श्रृंखला:Molecular Genetics & Genomic Medicine
विषय:
dilated cardiomyopathy
genetic modifier
genetics
sarcomere
ऑनलाइन पहुंच:https://doi.org/10.1002/mgg3.1049
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