Functional characterization of the novel DES mutation p.L136P associated with dilated cardiomyopathy reveals a dominant filament assembly defect-Reference-Cited by-同舟云学术

Functional characterization of the novel DES mutation p.L136P associated with dilated cardiomyopathy reveals a dominant filament assembly defect

Published:2016-02 Issue: Volume:91 Page:207-214
ISSN:0022-2828
Container-title:Journal of Molecular and Cellular Cardiology
language:en
Short-container-title:Journal of Molecular and Cellular Cardiology

Author:

Brodehl Andreas^ORCID,Dieding Mareike,Biere Niklas,Unger Andreas,Klauke Bärbel,Walhorn Volker,Gummert Jan,Schulz Uwe,Linke Wolfgang A.,Gerull Brenda,Vorgert Matthias,Anselmetti Dario,Milting Hendrik

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine,Molecular Biology

Reference53 articles.

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5. Exome sequencing and genome-wide linkage analysis in 17 families illustrate the complex contribution of TTN truncating variants to dilated cardiomyopathy;Norton;Circ. Cardiovasc. Genet.,2013

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