A Novel De Novo Dominant Mutation in GJB2 Gene Associated with a Sporadic Case of Nonsyndromic Sensorineural Hearing Loss

Mutations in the GJB2 gene are the most common known cause of hereditary congenital hearing loss. Rapid genomic DNA extraction (RGDE) method was used for genomic DNA extraction. After amplification of coding region of CX26 gene with specific primers, expected PCR products with 724bp length were subj...

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Detalles Bibliográficos
Autores principales: ONSORI, Habib, RAHMATI, Mohammad, FAZLI, Davood
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4499094/
https://www.ncbi.nlm.nih.gov/pubmed/26171365

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4499094/
https://www.ncbi.nlm.nih.gov/pubmed/26171365

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