Associated Papers
Subtle phenotypes of Mowat-Wilson syndrome in a patient with a novel ZEB2 C-ZF domain variant.
Kuroda Y et al.
American Journal of Medical Genetics. Part A, 2024
ZEB2 zinc-finger missense mutations lead to hypomorphic alleles and a mild Mowat-Wilson syndrome.
Ghoumid J et al.
Human Molecular Genetics, 2013
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