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Mutation analysis of the GJB2 and GJB6 genes in Egyptian patients with autosomal recessive sensorineural nonsyndromic hearing loss
Elbagoury, Nagham M., Soliman, Hala N., Mohammed, Ola S., Ghorab, Eman A., Elruby, Mona O., El-bassyouni, Hala T., Essawi, Mona L.Volume:
3
Language:
english
Journal:
Middle East Journal of Medical Genetics
DOI:
10.1097/01.MXE.0000438176.01557.b9
Date:
January, 2014
File:
PDF, 366 KB
english, 2014