Contribution of Common Variants in GABRG2, RELN and NRG3 and Interaction Networks to the Risk of Hirschsprung Disease | Zendy

Yang Wang | Zendy; Jun Wang | Zendy; Minghao Yin | Zendy; Zhiyun Wei | Zendy; Yongtao Xiao | Zendy; Kejun Zhou | Zendy; Jie Wen | Zendy; Junkai Yan | Zendy; Wei Cai | Zendy

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Contribution of Common Variants in GABRG2, RELN and NRG3 and Interaction Networks to the Risk of Hirschsprung Disease

Author(s) -

Yang Wang,

Jun Wang,

Minghao Yin,

Zhiyun Wei,

Yongtao Xiao,

Kejun Zhou,

Jie Wen,

Junkai Yan,

Wei Cai

Publication year - 2016

Publication title -

cellular physiology and biochemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 1.486

H-Index - 87

eISSN - 1421-9778

pISSN - 1015-8987

DOI - 10.1159/000452565

Subject(s) - biology , genetics , gene , haplotype , disease , genotype , medicine

Hirschsprung disease (HSCR) is a complex and heterogeneous disorder, characterized by a deficit in enteric nervous system. Genome-wide studies implied GABRG2, RELN and NRG3 might be involved in HSCR etiology. Here, we aimed to assess genetic variants in GABRG2, RELN and NRG3 that may confer susceptibility to HSCR and explore genetic interaction networks in HSCR.

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