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Δευτέρα 21 Μαΐου 2018

Frequency of mitochondrial m.1555A > G mutation in Syrian patients with non-syndromic hearing impairment

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 deficienc...

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