Biallelic loss of function variants in Myocardial zonula adherens protein gene (MYZAP) cause a severe recessive form of dilated cardiomyopathy
Author(s)
Type
Journal Article
Date Issued
2024-03
Date Acceptance
2024-03-01
Citation
Circulation: Heart Failure, 2024, 17 (3)
ISSN
1941-3289
Publisher
American Heart Association
Journal / Book Title
Circulation: Heart Failure
Volume
17
Issue
3
Copyright Statement
© 2024 The Authors. Circulation: Heart Failure is published on behalf of the American Heart Association, Inc., by Wolters Kluwer Health, Inc. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution, and reproduction in any medium, provided that the original work is properly cited.
License URL
Identifier
https://www.ncbi.nlm.nih.gov/pubmed/38436102
Subjects
Adherens Junctions
Cardiomyopathies
Cardiomyopathy, Dilated
Genetic Variation
Heart Failure
Humans
Phenotype
cardiomyopathies
dilated cardiomyopathy
human genetics
tachycardia, ventricular
whole exome sequencing
Publication Status
Published
Coverage Spatial
United States
Article Number
e011226
Date Publish Online
2024-03-04