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RET compound inheritance in Chinese patients with Hirschsprung disease: lack of penetrance from insufficient gene dysfunction

RET compound inheritance in Chinese patients with Hirschsprung disease: lack of penetrance from insufficient gene dysfunction
Author Jiang, Q; Wang, Y; Gao, Y; Wang, H; Zhang, Z; Li, Q; Xu, SH; Cai, W; Li, L
Journal HUMAN GENETICS
Pub Year
Type Article; Early Access
SCI 4.132