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Frequency of mitochondrial m.1555A > G mutation in Syrian patients with non-syndromic hearing impairment
BACKGROUND: Mitochondrial maternally inherited hearing impairment (HI) appears to be increasing in frequency. The incidence of mitochondrial defects causing HI is estimated to be between 6 and 33% of all hearing deficiencies. Mitochondrial m.1555A > G mutation is the first mtDNA mutation associat...
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| Publicado no: | BMC Ear Nose Throat Disord |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5963064/ https://ncbi.nlm.nih.gov/pubmed/29942192 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12901-018-0055-2 |
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