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

OBJECTIVE: To study connexin 26 (Cx26) gene mutations among autosomal recessive non-syndromal hearing loss in Kuwaiti patients and evaluate their effect on phenotypes. SUBJECTS AND METHODS: This cross sectional study included 100 patients aged between 6 months and 18 years, who were referred to the...

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Detalles Bibliográficos
Autores principales: Al-Sebeih, Khalid, Al-Kandari, Marium, Al-Awadi, Sadika A., Hegazy, Fatma F., Al-Khamees, Ghada A., Naguib, Kamal K., Al-Dabbous, Reem M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2013
Materias:
Original Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5586821/
https://www.ncbi.nlm.nih.gov/pubmed/24080506
http://dx.doi.org/10.1159/000348304

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5586821/
https://www.ncbi.nlm.nih.gov/pubmed/24080506
http://dx.doi.org/10.1159/000348304

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