Presentation of potential genes and deleterious variants associated with non-syndromic hearing loss: a computational approach

Non-syndromic hearing loss (NSHL) is a common hereditary disorder. Both clinical and genetic heterogeneity has created many obstacles to understanding the causes of NSHL. The present study has attempted to ravel the genetic aetiology in NSHL progression and to screen out potential target genes using...

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Detalles Bibliográficos
Autores principales: Ray, Manisha, Rath, Surya Narayan, Sarkar, Saurav, Sable, Mukund Namdev
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korea Genome Organization 2022
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9001992/
https://www.ncbi.nlm.nih.gov/pubmed/35399004
http://dx.doi.org/10.5808/gi.21070

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9001992/
https://www.ncbi.nlm.nih.gov/pubmed/35399004
http://dx.doi.org/10.5808/gi.21070

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