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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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Detalhes bibliográficos
Publicado no:Chin Med J (Engl)
Main Authors: Ju, Zhao-Ru, Wang, Hui-Jun, Ma, Xiao-Jing, Ma, Duan, Huang, Guo-Ying
Formato: Artigo
Idioma:Inglês
Publicado em: Medknow Publications & Media Pvt Ltd 2016
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5072250/
https://ncbi.nlm.nih.gov/pubmed/27748330
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0366-6999.191745
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