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...

Fuld beskrivelse

Na minha lista:
Bibliografiske detaljer
Udgivet i:J Cell Mol Med
Main Authors: Zhang, Yan, Xie, Xiaoli, Zeng, Jixiao, Wu, Qiang, Zhang, Ruizhong, Zhu, Deli, Xia, Huimin
Format: Artigo
Sprog:Inglês
Udgivet: John Wiley and Sons Inc. 2018
Fag:
Original Articles
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC5867083/
https://ncbi.nlm.nih.gov/pubmed/29377512
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/jcmm.13498
Tags: Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!

Lignende værker