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 development. SOX10 is a transcriptional regulator whose expression is essential in the developmen... https://www.hindigyanvishv.com/limited-stock-No-Face-No-Case-Logo-T-Shirt-special-save/