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...

Source: BMC Ear, Nose and Throat Disorders - May 21, 2018 Category: ENT & OMF Authors: Hazem Kaheel, Andreas Bre ß, Mohamed A. Hassan, Aftab Ali Shah, Mutaz Amin, Yousuf H. Y. Bakhit and Marlies Kniper Tags: Research article Source Type: research