TBX1 loss-of-function mutation contributes to congenital conotruncal defects

Conotruncal defects (CTDs) account for ~30% of all types of congenital heart disease and contribute to increased morbidity and mortality rates. Increasing evidence suggests that genetic risk factors are involved in the pathogenesis of CTDs. Mutations in a number of genes, including the TBX1 gene tha...

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Publicado en:Exp Ther Med
Autores principales: Zhang, Min, Li, Fu-Xing, Liu, Xing-Yuan, Hou, Jing-Yi, Ni, Shi-Hong, Wang, Juan, Zhao, Cui-Mei, Zhang, Wei, Kong, Ye, Huang, Ri-Tai, Xue, Song, Yang, Yi-Qing
Formato: Artigo
Lenguaje:Inglês
Publicado: D.A. Spandidos 2018
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Articles
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC5729719/
https://ncbi.nlm.nih.gov/pubmed/29250159
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/etm.2017.5362
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