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...

Descripción completa

Detalles Bibliográficos
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: Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3050791/
https://www.ncbi.nlm.nih.gov/pubmed/21349203
http://dx.doi.org/10.1186/1471-2350-12-32

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3050791/
https://www.ncbi.nlm.nih.gov/pubmed/21349203
http://dx.doi.org/10.1186/1471-2350-12-32

Ejemplares similares