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

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 den Wijngaard, Jan F. C. Glatz, Stephane R. B. Heymans, Ingrid P. C. Krapels, Shareef Nahas, Han G. Brunner, Radek Szklarczyk

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Original languageEnglish
Article numbere1049
Number of pages14
JournalMolecular genetics & genomic medicine
Volume8
Issue number2
Early online date27 Dec 2019
DOIs
Publication statusPublished - 8 Feb 2020

Keywords

  • dilated cardiomyopathy
  • genetic modifier
  • genetics
  • sarcomere
  • GENOME-WIDE ASSOCIATION
  • ENIGMA HOMOLOG
  • SEVERE FORM
  • VARIANTS
  • PROTEINS
  • LEADS

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