Genetic variants in RET and risk of Hirschsprung's disease in Southeastern Chinese: a haplotype-based analysis
<p>Abstract</p> <p>Background</p> <p>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...
Main Authors: | Gu Qinglong, Xiong Qixing, Liu Weiguang, Duan Shengyu, Zhong Rong, Wang Ying, Liu Li, Wang Li, Tou Jinfa, Yang Hong, Li Hui |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2011-02-01
|
Series: | BMC Medical Genetics |
Online Access: | http://www.biomedcentral.com/1471-2350/12/32 |
Similar Items
-
RET variants and haplotype analysis in a cohort of Czech patients with Hirschsprung disease.
by: Eliska Vaclavikova, et al.
Published: (2014-01-01) -
miRNA Profiling Reveals Dysregulation of RET and RET-Regulating Pathways in Hirschsprung's Disease.
by: Shuangshuang Li, et al.
Published: (2016-01-01) -
Whole Exome Sequencing Identifies a Novel Pathogenic RET Variant in Hirschsprung Disease
by: Wei Wu, et al.
Published: (2019-01-01) -
Neuroimmune regulation in Hirschsprung’s disease associated enterocolitis
by: Haosen Ji, et al.
Published: (2023-04-01) -
Functional Studies on Novel RET Mutations and Their Implications for Genetic Counseling for Hirschsprung Disease
by: Hui Wang, et al.
Published: (2019-10-01)