A Haplotype of Two Novel Polymorphisms in δ-Sarcoglycan Gene Increases Risk of Dilated Cardiomyopathy in Mongoloid Population-Reference-Cited by-同舟云学术

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A Haplotype of Two Novel Polymorphisms in δ-Sarcoglycan Gene Increases Risk of Dilated Cardiomyopathy in Mongoloid Population

Published:2015-12-31 Issue:12 Volume:10 Page:e0145602
ISSN:1932-6203
Container-title:PLOS ONE
language:en
Short-container-title:PLoS ONE

Author:

Chen Jie,Jin Ye,Wang Hong,Wei Sisi,Chen Dan,Ying Li,Zhou Qing,Li Gang,Li Joyce,Gao Jimin,Kato Naoya,Hu Wei,Li Yigang,Wang Yuepeng

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference45 articles.

1. Progress with genetic cardiomyopathies: screening, counseling, and testing in dilated, hypertrophic and arrhythmogenic right ventricular dysplasia/cardiomyopathy;RE Hershberger;Circ Heart Fail,2009

2. Hypertrophic cardiomyopathy in 2012;CY Ho;Circulation,2012

3. Genetic mutations and mechanisms in dilated cardiomyopathy;EM McNally;J Clin Invest,2013

4. Understanding cardiomyopathy phenotypes based on the functional impact of mutations in the myosin motor;JR Moore;Circ Res,2012

5. Mutation type is not clinically useful in predicting prognosis in hypertrophic cardiomyopathy;AP Landstrom;Circulation,2010

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2. Genetic considerations in cerebral small vessel diseases;Frontiers in Neurology;2023-04-24

3. Sarcoglycanopathies: Clinical, Molecular and Genetic Characteristics, Epidemiology, Diagnostics and Treatment Options;Russian Journal of Genetics;2018-02

4. Besides an ITIM/SHP-1-dependent pathway, CD22 collaborates with Grb2 and plasma membrane calcium-ATPase in an ITIM/SHP-1-independent pathway of attenuation of Ca2+i signal in B cells;Oncotarget;2016-06-02

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