Mitochondrial hearing loss mutations among Finnish preterm and term-born infants

Audiol Res. 2017 Nov 3;7(2):189. doi: 10.4081/audiores.2017.189. eCollection 2017 Jul 18.

¹ Faculty of Medicine, Arctic Health and Thule Institute, University of Oulu, Finland.

No abstract available

Keywords: MTRNR1; Mitochondrial DNA; aminoglycoside; infant; m.1095C>T; m.1494C>T; m.1555A>G; mtDNA; preterm; sensorineural hearing loss.