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...

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Main Authors: Gu Qinglong (Author), Xiong Qixing (Author), Liu Weiguang (Author), Duan Shengyu (Author), Zhong Rong (Author), Wang Ying (Author), Liu Li (Author), Wang Li (Author), Tou Jinfa (Author), Yang Hong (Author), Li Hui (Author)
Format: Book
Published: BMC, 2011-02-01T00:00:00Z.
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