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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Shranjeno v:
Bibliografske podrobnosti
izdano v:BMC Ear Nose Throat Disord
Main Authors: Kaheel, Hazem, Breß, Andreas, Hassan, Mohamed A., Shah, Aftab Ali, Amin, Mutaz, Bakhit, Yousuf H. Y., Kniper, Marlies
Format: Artigo
Jezik:Inglês
Izdano: BioMed Central 2018
Teme:
Research Article
Online dostop: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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