GJB2 c.−23+1G>A mutation is second most common mutation among Iranian individuals with autosomal recessive hearing loss

✍ Scribed by Zeinali, Sirous; Davoudi-Dehaghani, Elham; Azadmehr, Sarah; DabbaghBagheri, Samira; Bagherian, Hamideh; Jamali, Mojdeh; Zafarghandimotlagh, Fatemeh; Masoodifard, Mahboobeh; BandehiSarhaddi, Ameneh; Rejali, Leili; Sahebi, Sepideh

• Book ID: 125523377
• Publisher: Springer-Verlag
• Year: 2014
• Tongue: English
• Weight: 598 KB
• Volume: 272
• Category: Article
• ISSN: 0302-9530
• DOI: 10.1007/s00405-014-3171-7