Connexin 26 (GJB2) mutation in KID syndrome : an Egyptian patient
By: al-Sayyid, Sulaf M.; Sayf al-Din, Nifin S.; Bolz, Hanno. The Egyptian Journal of Medical Human Genetics. Vol. 12, no. 1 (2011), pp.91-93, 3 p.
Subjects: Deafness; Egypt; Diagnosis; Genetic aspects