Aberrant SOX10 and RET expressions in patients with Hirschsprung disease

HSCR is a complex genetic disorder characterized by the absence of ganglion cells in the intestine, leading to a functional obstruction. It is due to a disruption of complex signaling pathways within the gene ...

Source: BMC Pediatrics - March 16, 2024 Category: Pediatrics Authors: Gunadi, Verrell Christopher Amadeus, Fadila Dyah Trie Utami, Fiqih Vidiantoro Halim, Nabilah Anisa Novebri, Rahaditya Alrasyidi Hanggoro, Avinindita Nura Lestari, Kristy Iskandar, Andi Dwihantoro and Eko Purnomo Tags: Research Source Type: research