A founder variant expands the phenotype of WNT7B-related PDAC syndrome.
AlAbdi L, Rahbeeni Z, Maddirevula S, Helaby R, Abdulwahab F, Khan AO, Riley LG, Alhashem A, Chassaing N, Jamieson RV, Alkuraya FS.
AlAbdi L, et al. Among authors: alhashem a.
Clin Genet. 2024 Feb 28. doi: 10.1111/cge.14512. Online ahead of print.
Clin Genet. 2024.
PMID: 38417950