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...

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Bibliografische gegevens
Hoofdauteurs: 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
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Wiley 2020-02-01
Reeks:Molecular Genetics & Genomic Medicine
Onderwerpen:
dilated cardiomyopathy
genetic modifier
genetics
sarcomere
Online toegang:https://doi.org/10.1002/mgg3.1049
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