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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...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Korea Genome Organization
2022
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| Materias: | |
| 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 |