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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Asıl Yazarlar: Gu Qinglong (Yazar), Xiong Qixing (Yazar), Liu Weiguang (Yazar), Duan Shengyu (Yazar), Zhong Rong (Yazar), Wang Ying (Yazar), Liu Li (Yazar), Wang Li (Yazar), Tou Jinfa (Yazar), Yang Hong (Yazar), Li Hui (Yazar)
Materyal Türü: Kitap
Baskı/Yayın Bilgisi: BMC, 2011-02-01T00:00:00Z.
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3rd Floor Main Library

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Yer Numarası: A1234.567
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