Genetic variants in RET and risk of Hirschsprung's disease in Southeastern Chinese: a haplotype-based analysis

BACKGROUND: Hirschsprung's disease (HSCR) is a classic oligogenic disorder. Except inactivating mutations of RET, some single nucleotide polymorphisms (SNPs) are identified to be associated with the risk of HSCR. This study was conducted to examine the impact of the haplotypes profile of the re...

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Autores principales: Tou, Jinfa, Wang, Li, Liu, Li, Wang, Ying, Zhong, Rong, Duan, Shengyu, Liu, Weiguang, Xiong, Qixing, Gu, Qinglong, Yang, Hong, Li, Hui
Formato: Artigo
Lenguaje:Inglês
Publicado: BioMed Central 2011
Materias:
Research Article
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC3050791/
https://ncbi.nlm.nih.gov/pubmed/21349203
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-12-32
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