Analysis of Genetic Variations in Connexin 26 ( GJB2 ) Gene among Nonsyndromic Hearing Impairment: Familial Study

Objective  The goal of this research was to investigate the gap junction beta 2 ( GJB2 ) gene mutations associated with nonsyndromic hearing loss individuals in North Karnataka, India. Materials and Methods  For this study, patients with sensorineural genetic hearing abnormalities and a family histo...

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Detalles Bibliográficos
Autores principales: Hegde, Smita, Hegde, Rajat, Kulkarni, Suyamindra S., Das, Kusal K., Gai, Pramod B., Bulagouda, Rudragouda S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Georg Thieme Verlag KG 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9192169/
https://www.ncbi.nlm.nih.gov/pubmed/35707775
http://dx.doi.org/10.1055/s-0042-1743257

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9192169/
https://www.ncbi.nlm.nih.gov/pubmed/35707775
http://dx.doi.org/10.1055/s-0042-1743257

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