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Molecular diagnosis of SLC26A4-related hereditary hearing loss in a group of patients from two provinces of Iran
The SLC26A4 gene has been described as the second gene involved in most cases of autosomal recessive non-syndromic hearing loss (ARNSHL), after GJB2. Over 500 different SLC26A4 mutations have been reported, with each ethnic population having its own distinctive mutations. Here, we aimed to determine...
Sparad:
| I publikationen: | Intractable Rare Dis Res |
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| Huvudupphovsmän: | , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
International Research and Cooperation Association for Bio & Socio-Sciences Advancement
2021
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7882080/ https://ncbi.nlm.nih.gov/pubmed/33614372 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5582/irdr.2020.03090 |
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