TBX20 loss-of-function mutation responsible for familial tetralogy of Fallot or sporadic persistent truncus arteriosus

Congenital heart disease (CHD), the most common form of developmental abnormality in humans, remains a leading cause of morbidity and mortality in neonates. Genetic defects have been recognized as the predominant causes of CHD. Nevertheless, CHD is of substantial genetic heterogeneity and the geneti...

Ful tanımlama

Kaydedildi:
Detaylı Bibliyografya
Yayımlandı:Int J Med Sci
Asıl Yazarlar: Huang, Ri-Tai, Wang, Juan, Xue, Song, Qiu, Xing-Biao, Shi, Hong-Yu, Li, Ruo-Gu, Qu, Xin-Kai, Yang, Xiao-Xiao, Liu, Hua, Li, Ning, Li, Yan-Jie, Xu, Ying-Jia, Yang, Yi-Qing
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Ivyspring International Publisher 2017
Konular:
Research Paper
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC5436474/
https://ncbi.nlm.nih.gov/pubmed/28553164
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7150/ijms.17834
Etiketler: Etiketle
Etiket eklenmemiş, İlk siz ekleyin!

Benzer Materyaller