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Audiologic and Genetic Features of the A3243G mtDNA Mutation
Background: Mitochondrial mutations have been shown to be responsible for syndromic and nonsyndromic hearing impairment. Aim: To assess the genotypic–phenotypic correlation of mitochondrial DNA mutations in three generations of a single family. Methods: A single family with maternally inherited diab...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Mary Ann Liebert, Inc.
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3634140/ https://ncbi.nlm.nih.gov/pubmed/23477312 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1089/gtmb.2012.0403 |
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