Identification of epigenetic factor KAT2B gene variants for possible roles in congenital heart diseases

Congenital heart disease (CHD) is a group of anatomic malformations in the heart with high morbidity and mortality. The mammalian heart is a complex organ, the formation and development of which are strictly regulated and controlled by gene regulatory networks of many signaling pathways such as TGF-...

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Detalles Bibliográficos
Autores principales: Hou, Yong-Sheng, Wang, Jing-Zhi, Shi, Shuai, Han, Ying, Zhang, Yue, Zhi, Ji-Xin, Xu, Chao, Li, Fei-Feng, Wang, Gui-Yu, Liu, Shu-Lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2020
Materias:
Diagnostics & Biomarkers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7160239/
https://www.ncbi.nlm.nih.gov/pubmed/32239175
http://dx.doi.org/10.1042/BSR20191779

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7160239/
https://www.ncbi.nlm.nih.gov/pubmed/32239175
http://dx.doi.org/10.1042/BSR20191779

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