Associated Papers
A Missense Variant in the IKZF2 Gene Identified in a Genetically Undiagnosed Family With Hearing Loss.
Zhang T et al.
American Journal of Medical Genetics. Part A, 2025
Exome variant prioritization in a large cohort of hearing-impaired individuals indicates IKZF2 to be associated with non-syndromic hearing loss and guides future research of unsolved cases.
Velde HM et al.
Human Genetics, 2024
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