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Phenotypic expression of maternally inherited deafness is affected by RNA modification and cytoplasmic ribosomal proteins
The homoplasmic mitochondrial A1555G mutation in the 12S rRNA gene leads to a mitochondrial translation disorder associated with deafness. The absence of disease in non-cochlear tissues in all patients, and in the cochlea in some patients, is not well understood. We used a system-based approach, inc...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2009
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2728627/ https://ncbi.nlm.nih.gov/pubmed/19482502 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ymgme.2009.05.003 |
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