Detection of 35delG, 167delT mutations in the connexin 26 gene among Egyptian patients with nonsyndromic sensorineural hearing loss

En Aim The aim of this study was to detect 35delG and 167delT mutations in the connexin 26 gene among Egyptian patients with nonsyndromic sensorineural hearing loss, allowing accurate diagnosis, proper genetic counseling, and carrier detection. Patients and methods Fifty-one patients were subjected...

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Veröffentlicht in:	The Egyptian journal of otolaryngology 2015, Vol.31 (1), p.42-46
Hauptverfasser:	El Barbary, Nehal E., El Belbesy, Mervat F., Asal, Samir I., Kholeif, Soha F.
Format:	Artikel
Sprache:	eng
Schlagworte:	Medicine & Public Health Original Article Surgery
Online-Zugang:	Volltext
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