GJB2 c.−23+1G>A mutation is second most common mutation among Iranian individuals with autosomal recessive hearing loss
Crossref DOI link: https://doi.org/10.1007/s00405-014-3171-7
Published Online: 2014-07-11
Published Print: 2015-09
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Zeinali, Sirous
Davoudi-Dehaghani, Elham
Azadmehr, Sarah
DabbaghBagheri, Samira
Bagherian, Hamideh
Jamali, Mojdeh
Zafarghandimotlagh, Fatemeh
Masoodifard, Mahboobeh
BandehiSarhaddi, Ameneh
Rejali, Leili
Sahebi, Sepideh
Text and Data Mining valid from 2014-07-11