Association of NRG1 and AUTS2 genetic polymorphisms with Hirschsprung disease in a South Chinese population

Hirschsprung disease (HSCR) is a genetic disorder characterized by the absence of enteric ganglia. There are more than 15 genes identified as contributed to HSCR by family‐based or population‐based approaches. However, these findings were not fulfilled to explain the heritability of most sporadic ca...

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Detalles Bibliográficos
Autores principales: Zhang, Yan, Xie, Xiaoli, Zeng, Jixiao, Wu, Qiang, Zhang, Ruizhong, Zhu, Deli, Xia, Huimin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5867083/
https://www.ncbi.nlm.nih.gov/pubmed/29377512
http://dx.doi.org/10.1111/jcmm.13498

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5867083/
https://www.ncbi.nlm.nih.gov/pubmed/29377512
http://dx.doi.org/10.1111/jcmm.13498

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