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An MRPS12 mutation modifies aminoglycoside sensitivity caused by 12S rRNA mutations
Several homoplasmic pathologic mutations in mitochondrial DNA, such as those causing Leber hereditary optic neuropathy or non-syndromic hearing loss, show incomplete penetrance. Therefore, other elements must modify their pathogenicity. Discovery of these modifying factors is not an easy task becaus...
में बचाया:
| में प्रकाशित: | Front Genet |
|---|---|
| मुख्य लेखकों: | , , , , , , , |
| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
Frontiers Media S.A.
2015
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| विषय: | |
| ऑनलाइन पहुंच: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4294204/ https://ncbi.nlm.nih.gov/pubmed/25642242 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2014.00469 |
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