Biallelic Loss of Function Variants in Myocardial Zonula Adherens Protein Gene (MYZAP) Cause a Severe Recessive Form of Dilated Cardiomyopathy.

Journal: Circulation. Heart failure

Volume: 17

Issue: 3

Year of Publication: 2024

Affiliated Institutions:  Hospital Universitario Puerta de Hierro Majadahonda, IDIPHISA, Madrid, Spain (J.P.O., J.G.M., F.D., E.G.-L., C.S., G.R., P.G.-P.). Centro Nacional de Investigaciones Cardiovasculares, Madrid, Spain (J.P.O., L.L., F.D., E.G.-L., E.L.-P., P.G.-P.). National Heart and Lung Institute (K.A.M, S.L.Z., P.J.R.B., J.S.W.), Imperial College London, United Kingdom. Instituto de Investigación Sanitaria Gregorio Marañón, Madrid, Spain (M.V.G.-G.). CIBERCV, Instituto de Salud Carlos III, Madrid, Spain (J.P.O., F.D., E.G.-L., C.S., E.L.-P., P.G.-P.).

Abstract summary 

Authors & Co-authors:  Ochoa Lalaguna Mirelis Dominguez Gonzalez-Lopez Salas Roustan McGurk Zheng Barton Ware Gómez-Gaviro Lara-Pezzi Garcia-Pavia

Study Outcome 

Source Link: Visit source

Statistics
Citations :  Escobar-Lopez L, Ochoa JP, Mirelis JG, Espinosa MA, Navarro M, Gallego-Delgado M, Barriales-Villa R, Robles-Mezcua A, Basurte-Elorz MT, Gutiérrez García-Moreno L, et al. . Association of genetic variants with outcomes in patients with nonischemic dilated cardiomyopathy. J Am Coll Cardiol. 2021;78:1682–1699. doi: 10.1016/j.jacc.2021.08.039
Authors :  14
Identifiers
Doi : 10.1161/CIRCHEARTFAILURE.123.011226
SSN : 1941-3297
Study Population
Male,Female
Mesh Terms
Humans
Other Terms
cardiomyopathies;dilated cardiomyopathy;human genetics;tachycardia, ventricular;whole exome sequencing
Study Design
Study Approach
Country of Study
Publication Country
United States