Identification and Computational Analysis of Rare Variants of Known Hearing Loss Genes Present in Five Deaf Members of a Pakistani Kindred

Hearing loss (HL) is the most common neurosensory defect in humans that affects the normal communication. Disease is clinically and genetically heterogeneous, rendering challenges for the molecular diagnosis of affected subjects. This study highlights the phenotypic and genetic complexity of inherit...

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Detalles Bibliográficos
Autores principales: Saleem, Irum Badshah, Masoud, Muhammad Shareef, Qasim, Muhammad, Ali, Muhammad, Ahmed, Zubair M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Brief Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8702217/
https://www.ncbi.nlm.nih.gov/pubmed/34946889
http://dx.doi.org/10.3390/genes12121940

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8702217/
https://www.ncbi.nlm.nih.gov/pubmed/34946889
http://dx.doi.org/10.3390/genes12121940

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