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
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