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Hearing Phenotypes of Patients with Hearing Loss Homozygous for the GJB2 c.235delc Mutation
Hereditary hearing loss is characterized by remarkable phenotypic heterogeneity. Patients with the same pathogenic mutations may exhibit various hearing loss phenotypes. In the Chinese population, the c.235delC mutation is the most common pathogenic mutation of GJB2 and is closely related to heredit...
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| Pubblicato in: | Neural Plast |
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| Autori principali: | , , , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Hindawi
2020
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7416285/ https://ncbi.nlm.nih.gov/pubmed/32802038 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2020/8841522 |
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