Whole-Exome Sequencing Reveals a Rare Variant of OTOF Gene Causing Congenital Non-syndromic Hearing Loss Among Large Muslim Families Favoring Consanguinity

Non-syndromic hearing loss (NSHL) is one of the most frequent auditory deficits in humans characterized by high clinical and genetic heterogeneity. Very few studies have reported the relationship between OTOF (Locus: DFNB9) and hereditary hearing loss in India. We aimed to decipher the genetic cause...

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Detalles Bibliográficos
Autores principales: Fareed, Mohd, Sharma, Varun, Singh, Inderpal, Rehman, Sayeed Ur, Singh, Gurdarshan, Afzal, Mohammad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8185570/
https://www.ncbi.nlm.nih.gov/pubmed/34113375
http://dx.doi.org/10.3389/fgene.2021.641925

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8185570/
https://www.ncbi.nlm.nih.gov/pubmed/34113375
http://dx.doi.org/10.3389/fgene.2021.641925

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