Deafness gene variations in a 1120 nonsyndromic hearing loss cohort: molecular epidemiology and deafness mutation spectrum of patients in Japan.
The Annals of otology, rhinology, and laryngology 2015 May 124 Suppl 1 49S-60S.
Nishio Shin-Ya, Usami Shin-Ic
Genetic causes of nonsyndromic hearing loss in Iran in comparison with other populations.
Journal of human genetics 2010 Oct 55 (10): 639-48.
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