A Novel Mutation in the GJB2 (Connexin 26) Gene in Egyptian Children with Non-syndromic Sensorineural Hearing Loss Journal title: Macedonian Journal of Medical Sciences (MJMS) Authors: Nagwa Meguid| National Research Center - Research on Children with Special Needs Department, Giza, E... Subject(s): Epidemiology, Physiology
GJB2 sequencing in deaf and profound sensorineural hearing loss children Journal title: Otolaryngologia Polska Authors: Marzena Mielczarek, Anna Zakrzewska, Jurek Olszewski Subject(s):
