Genetic polymorphisms of the SOX10 gene in Thai patients with sporadic Hirschsprung disease

Genetic polymorphisms of the SOX10 gene in Thai patients with sporadic Hirschsprung disease

Hirschsprung disease (HSCR) is complex genetic disorder of the enteric nervous system (ENS) characterized by an absence of ganglion cells in various parts of the intestine. The disease has a strong genetic association with RET-protooncogene (RET) and various genes involved in neural crest developm...

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Bibliographic Details
Main Authors:	Karun Eadyow, Theerawut Phusantisampan, Wanwisa Maneechay, Surasak Sangkhathat
Format:	Article
Language:	English
Published:	Prince of Songkla University 2020-06-01
Series:	Songklanakarin Journal of Science and Technology (SJST)
Subjects:	hirschsprung disease (hscr) ganglion cells single nucleotide polymorphisms (snps) sox10 ret-protooncogene
Online Access:	https://rdo.psu.ac.th/sjstweb/journal/42-3/14.pdf

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