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...
| Main Authors: | , , , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Prince of Songkla University
2020-06-01
|
| Series: | Songklanakarin Journal of Science and Technology (SJST) |
| Subjects: | |
| Online Access: | https://rdo.psu.ac.th/sjstweb/journal/42-3/14.pdf |