High frequency of the deafness-associated 167delT mutation in the connexin 26 (GJB2) gene in Israeli Ashkenazim

1999/10/29 by Tama Sobe, Porat Erlich, Porat M. Erlich +6 · 3 citations
Biochemistry, Genetics and Molecular Biology · Neuroscience · #Connexins and lens biology #Hearing, Cochlea, Tinnitus, Genetics #Neuroscience of respiration and sleep

paper · doi:10.1002/(sici)1096-8628(19991029)86:5<499::aid-ajmg19>3.0.co;2-o

openalex publication_date 1999/10/29 · openalex created_date 2025/10/10 · openalex updated_date 2026/07/22

Cited by

• GJB2 (connexin 26) variants and nonsyndromic sensorineural hearing loss: A HuGE review
• A deletion mutation in GJB6 cooperating with a GJB2 mutation in trans in non-syndromic deafness: A novel founder mutation in Ashkenazi Jews
• Connexin 26 and Connexin 30 Mutations in Children with Nonsyndromic Hearing Loss