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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Detalles Bibliográficos
Autores principales: Ju, Zhao-Ru, Wang, Hui-Jun, Ma, Xiao-Jing, Ma, Duan, Huang, Guo-Ying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2016
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5072250/
https://www.ncbi.nlm.nih.gov/pubmed/27748330
http://dx.doi.org/10.4103/0366-6999.191745

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5072250/
https://www.ncbi.nlm.nih.gov/pubmed/27748330
http://dx.doi.org/10.4103/0366-6999.191745

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