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Article

Associations of CYP2B6 genetic polymorphisms with Hirschsprung's disease in a southern Chinese population.

Journal of clinical laboratory analysis - 1 Dec 2021

Liu Yanqing, Lan Chaoting, Li Bingxiao, Wang Ning, Zuo Xiaoyu, Huang Lihua, Wu Yuxin, Zhu Yun

Abstract excerpt

BACKGROUND: Hirschsprung's disease (HSCR) is an enteric nervous system birth defect partially caused by a genetic disorder. Single-nucleotide polymorphisms (SNPs) of the cytochrome P450 family 2 subfamily B member 6 (CYP2B6) gene are reported to be associated with HSCR. METHODS: We evaluated the association of rs2054675, rs707265, and rs1042389 with HSCR susceptibility in southern Chinese children including 1470...

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PMID: 34752660
DOI: 10.1002/jcla.24074
PMCID: PMC8649360

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