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...

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Detalles Bibliográficos
Autores principales: Al-Kindi, Mohammed Nasser, Al-Khabouri, Mazin Jawad, Al-Lamki, Khalsa Ahmad, Palombo, Flavia, Pippucci, Tommaso, Romeo, Giovanni, Al-Wardy, Nadia Mohammed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2020
Materias:
Research
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

Internet

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

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