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Clinical characteristics with long-term follow-up of four Okinawan families with moderate hearing loss caused by an OTOG variant
We describe the clinical features of four Japanese families with moderate sensorineural hearing loss due to the OTOG gene variant. We analyzed 98 hearing loss-related genes in patients with hearing loss originally from the Okinawa Islands using next-generation sequencing. We identified a homozygous...
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| Pubblicato in: | Hum Genome Var |
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| Autori principali: | , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Nature Publishing Group UK
2019
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6804730/ https://ncbi.nlm.nih.gov/pubmed/31645975 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41439-019-0068-4 |
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