Associated Papers
Auditory Phenotype of a Novel Missense Variant in the CEACAM16 Gene in a Large Russian Family With Autosomal Dominant Nonsyndromic Hearing Loss.
Markova TG et al.
The Journal of International Advanced Otology, 2024
Old gene, new phenotype: splice-altering variants in CEACAM16 cause recessive non-syndromic hearing impairment.
Booth KT et al.
Journal of Medical Genetics, 2018
A Novel de novo Mutation in CEACAM16 Associated with Postlingual Hearing Impairment.
Hofrichter MA et al.
Molecular Syndromology, 2015
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