Highly recurrent RET mutations and novel mutations in genes of the receptor tyrosine kinase and endothelin receptor B pathways in Chinese patients with sporadic Hirschsprung disease.

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DOI:10.1373/clinchem.2003.022061
作者：Mercè Garcia-Barceló, Mai-Har Sham, Wing-Shan Lee, Vincent Chi-Hang Lui, Benedict Ling-Sze Chen, Kenneth Kak-Yuen Wong, Joyce Suet-Wan Wong, Paul Kwong-Hang Tam
文献类型：期刊论文
补充材料：只需要正文
文献链接：https://doi.org/10.1373/clinchem.2003.022061

Oxford University Press

Abstract：Background: Hirschsprung disease (HSCR) is a congenital disorder characterized by an absence of ganglion cells in the nerve plexuses of the lower digestive tract. HSCR has a complex pattern

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