Genetic association and functional validation of ZFP36L2 in non-syndromic orofacial cleft subtypes

ConclusionOur findings highlight the significance ofZFP36L2 in the etiology of NSOC, supported by both human genetic association data and functional studies in zebrafish. These results pave the way for further exploration of targeted interventions for craniofacial malformations.
Source: Journal of Human Genetics - Category: Genetics & Stem Cells Source Type: research