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Mutation spectrum of non‐syndromic hearing loss in the UAE, a retrospective cohort study and literature review
BACKGROUND: Hearing loss (HL) is a heterogeneous condition that causes partial or complete hearing impairment. Hundreds of variants in >60 genes have been reported to be associated with Hereditary HL (HHL), variants of the GJB2 gene are the most common cause of congenital SNHL, with >100 varia...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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John Wiley and Sons Inc.
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9651598/ https://www.ncbi.nlm.nih.gov/pubmed/36056583 http://dx.doi.org/10.1002/mgg3.2052 |