A de novo Mutation in the MTUS1 Gene Decreases the Risk of Non-compaction of Ventricular Myocardium via the Rac1/Cdc42 Pathway-Reference-Cited by-同舟云学术

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A de novo Mutation in the MTUS1 Gene Decreases the Risk of Non-compaction of Ventricular Myocardium via the Rac1/Cdc42 Pathway

Published:2019-07-02 Issue: Volume:7 Page:
ISSN:2296-2360
Container-title:Frontiers in Pediatrics
language:
Short-container-title:Front. Pediatr.

Author:

Bai Xuehan,Zhou Yuanlin,Ouyang Na,Liu Lingjuan,Huang Xupei,Tian Jie,Lv Tiewei

Funder

National Natural Science Foundation of China

Publisher

Frontiers Media SA

Subject

Pediatrics, Perinatology, and Child Health

Reference39 articles.

1. Classification of the cardiomyopathies: a position statement from the European Society Of Cardiology Working Group on Myocardial and Pericardial Diseases;Elliott;Eur Heart J.,2008

2. Heuristic problems in defining the three-dimensional arrangement of the ventricular myocytes;Anderson;Anat Rec A Discov Mol Cell Evol Biol.,2006

3. Classification of cardiomyopathies and indication for endomyocardial biopsy revisited;Pankuweit;Herz.,2009

4. Mutations in the NOTCH pathway regulator MIB1 cause left ventricular noncompaction cardiomyopathy;Luxan;Nat Med.,2013

5. Clinical features of isolated ventricular noncompaction in adults long-term clinical course, echocardiographic properties, and predictors of left ventricular failure;Aras;J Card Fail.,2006

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