Rare mutations in apoptosis related genes APAF1, CASP9, and CASP3 contribute to human neural tube defects

Detalles Bibliográficos
Autores principales: Zhou, Xiangyu, Zeng, Weijia, Li, Huili, Chen, Haitao, Wei, Gang, Yang, Xueyan, Zhang, Ting, Wang, Hongyan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Correspondence
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5833651/
https://www.ncbi.nlm.nih.gov/pubmed/29352212
http://dx.doi.org/10.1038/s41419-017-0096-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5833651/
https://www.ncbi.nlm.nih.gov/pubmed/29352212
http://dx.doi.org/10.1038/s41419-017-0096-2

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