HIRA Gene is Lower Expressed in the Myocardium of Patients with Tetralogy of Fallot

HIRA Gene is Lower Expressed in the Myocardium of Patients with Tetralogy of Fallot

Background: The most typical cardiac abnormality is conotruncal defects (CTDs) in patients with 22q11 deletion syndrome (22q11DS). HIRA (histone cell cycle regulator) gene, as one of the candidate genes located at the critical region of 22q11DS, was reported as possibly relevant to CTD in animal mod...

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Bibliographic Details
Main Authors: Zhao-Ru Ju, Hui-Jun Wang, Xiao-Jing Ma, Duan Ma, Guo-Ying Huang
Format: Article
Language:English
Published: Wolters Kluwer 2016-01-01
Series:Chinese Medical Journal
Subjects:
Congenital Heart Defects; Gene Expression; HIRA; Single Nucleotide Polymorphism; Tetralogy of Fallot
Online Access:http://www.cmj.org/article.asp?issn=0366-6999;year=2016;volume=129;issue=20;spage=2403;epage=2408;aulast=Ju

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http://www.cmj.org/article.asp?issn=0366-6999;year=2016;volume=129;issue=20;spage=2403;epage=2408;aulast=Ju

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