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Analysis of mitochondrial A1555G mutation in infants with hearing impairment
Mutations in the mitochondrial 12S ribosomal RNA gene have been identified to be associated with deafness. Among these, the A to G transition at position 1555 is one of the most common pathogenic mutations associated with hearing loss. In order to evaluate the allele frequency of this mutation in in...
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| Publicat a: | Exp Ther Med |
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| Autors principals: | , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
D.A. Spandidos
2018
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5958681/ https://ncbi.nlm.nih.gov/pubmed/29805548 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/etm.2018.6078 |
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