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Mutations in LOXHD1 gene cause various types and severities of hearing loss
OBJECTIVE: We present two families that were identified with novel mutations in LOXHD1, as a cause of non-progressive hearing loss. METHODS: One thousand three hundred fourteen (1,314) Japanese subjects with sensorineural hearing loss from unrelated families were enrolled in the study. Targeted geno...
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| Publicat a: | Ann Otol Rhinol Laryngol |
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| Autors principals: | , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2015
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4441841/ https://ncbi.nlm.nih.gov/pubmed/25792669 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/0003489415574067 |
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