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Connexin 26 Gene Mutations in Non-Syndromic Hearing Loss Among Kuwaiti Patients

✍ Scribed by Al-Sebeih, Khalid; Al-Kandari, Marium; Al-Awadi, Sadika A.; Hegazy, Fatma F.; Al-Khamees, Ghada A.; Naguib, Kamal K.; Al-Dabbous, Reem M.

Book ID
121262069
Publisher
S. Karger AG
Year
2014
Tongue
English
Weight
114 KB
Volume
23
Category
Article
ISSN
1011-7571

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Congenital sensorineural hearing loss affects approximately 1/1,000 live births. Mutations in the gene encoding connexin26 (GJB2) have been described as a major cause of genetic nonsyndromic hearing impairment. Additionally, another gap junction gene, connexin30 (GJB6), was found to be responsible f