PLEKHM2mutation leads to abnormal localization of lysosomes, impaired autophagy flux and associates with recessive dilated cardiomyopathy and left ventricular noncompaction-Reference-Cited by-同舟云学术

PLEKHM2mutation leads to abnormal localization of lysosomes, impaired autophagy flux and associates with recessive dilated cardiomyopathy and left ventricular noncompaction

Published:2015-10-12 Issue:25 Volume:24 Page:7227-7240
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Hum. Mol. Genet.

Author:

Muhammad Emad,Levitas Aviva,Singh Sonia R.,Braiman Alex,Ofir Rivka,Etzion Sharon,Sheffield Val C.,Etzion Yoram,Carrier Lucie,Parvari Ruti

Funder

Ben-

Gurion University

Negev, Faculty of Health Sciences

Leducq Foundation

Howard Hughes Medical Institute

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/24/25/7227/17262463/ddv423.pdf

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3. Where Genome Meets Phenome: Rationale for Integrating Genetic and Protein Biomarkers in the Diagnosis and Management of Dilated Cardiomyopathy and Heart Failure

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