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Hearing consequences in Gjb2 knock-in mice: implications for human p.V37I mutation
Human p.V37I mutation of GJB2 gene was strongly correlated with late-onset progressive hearing loss, especially among East Asia populations. We generated a knock-in mouse model based on human p.V37I variant (c.109G>A) that recapitulated the human phenotype. Cochlear pathology revealed no signific...
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| Publicat a: | Aging (Albany NY) |
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| Autors principals: | , , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Impact Journals
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6782001/ https://ncbi.nlm.nih.gov/pubmed/31562289 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.18632/aging.102246 |
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