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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Detalles Bibliográficos
Autores principales: Kaheel, Hazem, Breß, Andreas, Hassan, Mohamed A., Shah, Aftab Ali, Amin, Mutaz, Bakhit, Yousuf H. Y., Kniper, Marlies
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5963064/
https://www.ncbi.nlm.nih.gov/pubmed/29942192
http://dx.doi.org/10.1186/s12901-018-0055-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5963064/
https://www.ncbi.nlm.nih.gov/pubmed/29942192
http://dx.doi.org/10.1186/s12901-018-0055-2

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