Associated Papers
Identification and functional analysis of biallelic loss-of-function variants of WNT7B in a Chinese family affected with PDAC syndrome.
Qiu L et al.
Gene, 2026
A founder variant expands the phenotype of WNT7B-related PDAC syndrome.
AlAbdi L et al.
Clinical Genetics, 2024
Bi-allelic variants in WNT7B disrupt the development of multiple organs in humans.
Bouasker S et al.
Journal of Medical Genetics, 2023
Shared and divergent contribution of vitamin A and oxytocin to the aetiology of autism spectrum disorder.
Wang T et al.
Computational and Structural Biotechnology Journal, 2023
38213898 (PubMed )
Supplement: mmc2.xlsx › RIVs_in_VARGs
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