Common genetic variants in GAL, GAP43 and NRSN1 and interaction networks confer susceptibility to Hirschsprung disease

Hirschsprung disease (HSCR) is a severe multifactorial genetic disorder. Microarray studies indicated GAL,GAP43 and NRSN1 might contribute to the altered risk in HSCR. Thus, we focused on genetic variations in GAL,GAP43 and NRSN1, and the gene‐gene interactions involved in HSCR susceptibility. We re...

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Publicat a:J Cell Mol Med
Autors principals: Wang, Yang, Yan, Weihui, Wang, Jun, Zhou, Ying, Chen, Jie, Gu, Beilin, Cai, Wei
Format: Artigo
Idioma:Inglês
Publicat: John Wiley and Sons Inc. 2018
Matèries:
Original Articles
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6010875/
https://ncbi.nlm.nih.gov/pubmed/29654647
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/jcmm.13612
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