The Analysis of GJB2, GJB3, and GJB6 Gene Mutations in Patients with Hereditary Non-Syndromic Hearing Loss Living in Sivas.

Küçük Kurtulgan, Hande

The Analysis of GJB2, GJB3, and GJB6 Gene Mutations in Patients with Hereditary Non-Syndromic Hearing Loss Living in Sivas. [electronic resource] - The journal of international advanced otology Dec 2019 - 373-378 p. digital

Publication Type: Journal Article

2148-3817

10.5152/iao.2019.5401 doi


Adolescent
Adult
Aged
Child
Child, Preschool
Connexin 26
Connexin 30--genetics
Connexins--genetics
Consanguinity
Female
Gene Frequency
Genotype
Hearing Loss, Sensorineural--genetics
Heterozygote
Homozygote
Humans
Male
Middle Aged
Mutation
Turkey
Young Adult