Investigation of the mtDNA mutations in Syrian families with non-syndromic sensorineural hearing loss.

Moassass, Faten

Investigation of the mtDNA mutations in Syrian families with non-syndromic sensorineural hearing loss. [electronic resource] - International journal of pediatric otorhinolaryngology Oct 2018 - 110-114 p. digital

Publication Type: Journal Article

1872-8464

10.1016/j.ijporl.2018.07.028 doi


Adolescent
Child
Child, Preschool
DNA, Mitochondrial--genetics
Female
Genotype
Hearing Loss, Sensorineural--genetics
Humans
Male
Mutation
Syria