MEF2C loss-of-function mutation contributes to congenital heart defects

Congenital heart disease (CHD) is the most common type of developmental abnormality in humans, and is a leading cause for substantially increased morbidity and mortality in affected individuals. Increasing studies demonstrates a pivotal role of genetic defects in the pathogenesis of CHD, and present...

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Detalles Bibliográficos
Autores principales: Qiao, Xiao-Hui, Wang, Fei, Zhang, Xian-Ling, Huang, Ri-Tai, Xue, Song, Wang, Juan, Qiu, Xing-Biao, Liu, Xing-Yuan, Yang, Yi-Qing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2017
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5666546/
https://www.ncbi.nlm.nih.gov/pubmed/29104469
http://dx.doi.org/10.7150/ijms.21353

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5666546/
https://www.ncbi.nlm.nih.gov/pubmed/29104469
http://dx.doi.org/10.7150/ijms.21353

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