Whole-exome sequencing to identify the cause of congenital sensorineural hearing loss in carriers of a heterozygous GJB2 mutation.

Name: Whole-exome sequencing to identify the cause of congenital sensorineural hearing loss in carriers of a heterozygous GJB2 mutation.
Author: Parzefall, Thomas

Whole-exome sequencing to identify the cause of congenital sensorineural hearing loss in carriers of a heterozygous GJB2 mutation. — المؤلف: Parzefall, Thomas — European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the Ge

المؤلف: Parzefall, Thomas
النشر: European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery 20180529
الوصف: 3619-3625 p.
الموضوعات: Adult؛ Austria؛ Connexin 26؛ Connexins؛ Female؛ Genetic Testing؛ Hearing Loss, Sensorineural؛ Humans