GJB2 c.−23+1G>A mutation is second most common mutation among Iranian individuals with autosomal recessive hearing loss
Zeinali, Sirous, Davoudi-Dehaghani, Elham, Azadmehr, Sarah, DabbaghBagheri, Samira, Bagherian, Hamideh, Jamali, Mojdeh, Zafarghandimotlagh, Fatemeh, Masoodifard, Mahboobeh, BandehiSarhaddi, Ameneh, ReVolume:
272
Language:
english
Journal:
European Archives of Oto-Rhino-Laryngology
DOI:
10.1007/s00405-014-3171-7
Date:
September, 2015
File:
PDF, 598 KB
english, 2015