P288: SIX1 c.396G>C (p.Lys132Asn) in a UAE family with autosomal dominant hearing loss reveals regional diagnostic gaps

Genetics in Medicine Open 2026 Open access

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Authors: Khola Younus Haji Ibrahim, Abdullah Al Mutery
DOI: 10.1016/j.gimo.2026.103782
Cited by: 0

Fields of Study & Subjects

Hearing Cochlea Tinnitus Genetics Genomics and Rare Diseases Hereditary Neurological Disorders

Publication details

Journal / source
Genetics in Medicine Open
Volume
4
Pages
103782–103782
Publication date
1 January 2026
Language
EN