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Screening for the mitochondrial A1555G mutation among Egyptian patients with non-syndromic, sensorineural hearing loss
Background & Aim: Hearing loss is the most frequent form of neurosensory deficit in humans. Although the majority of hereditary hearing loss is due to nuclear gene mutations, it has become clear the significant contribution of mitochondrial genes. The first mitochondrial mutation shown to cause...
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| Publicat a: | Int J Mol Epidemiol Genet |
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| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
e-Century Publishing Corporation
2014
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4348701/ https://ncbi.nlm.nih.gov/pubmed/25755848 |
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