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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Detaylı Bibliyografya
Yayımlandı:J Cell Mol Med
Asıl Yazarlar: Zhang, Yan, Xie, Xiaoli, Zeng, Jixiao, Wu, Qiang, Zhang, Ruizhong, Zhu, Deli, Xia, Huimin
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: John Wiley and Sons Inc. 2018
Konular:
Original Articles
Online Erişim: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
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