Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Hirschsprung Disease and GAP43[original query] |
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Common genetic variants in GAL, GAP43 and NRSN1 and interaction networks confer susceptibility to Hirschsprung disease. Journal of cellular and molecular medicine 2018 Apr . Wang Yang, Yan Weihui, Wang Jun, Zhou Ying, Chen Jie, Gu Beilin, Cai W |
Genetic variants in RET, ARHGEF3 and CTNNAL1, and relevant interaction networks, contribute to the risk of Hirschsprung disease. Aging 2020 3 12 (5): 4379-4393. Wang Yang, Jiang Qian, Cai Hao, Xu Ze, Wu Wenjie, Gu Beilin, Li Long, Cai W |
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