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In silico analysis of a novel causative mutation in Cadherin23 gene identified in an Omani family with hearing loss
BACKGROUND: Hereditary hearing loss is a heterogeneous group of complex disorders with an overall incidence of one in every 500 newborns presented as syndromic and non-syndromic forms. Cadherin-related 23 (CDH23) is one of the listed deafness causative genes. It is found to be expressed in the stere...
| Autores principales: | , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Springer Berlin Heidelberg
2020
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7049540/ https://www.ncbi.nlm.nih.gov/pubmed/32115674 http://dx.doi.org/10.1186/s43141-020-0021-4 |