Open access
Aug 2026
A Novel Loss-of-Function Variant in TGFBI Associated with Non-Syndromic Orofacial Clefts in a Chinese Pedigree
This study identifies a rare loss-of-function TGFBI variant associated with NSOFCs and provides genetic and functional evidence supporting a role for TGFBI variation in human palatal development.
Shu-Jie Hou, Siang Li, Xin-Luo Wang et al.
· Genes · 0 citations