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1.
GJB2 and mitochondrial A1555G gene mutations in nonsyndromic profound hearing loss and carrier frequencies in healthy individuals
作者:
Elif Baysal (1)
Yildirim A. Bayazit (1)
Serdar Ceylaner (2)
Necat
Alatas
(3)
Buket Donmez (2)
Gulay Ceylaner (2)
Imran San (3)
Baki Korkmaz (3)
Akin Yilmaz (4)
Adnan Menevse (4)
Senay Altunyay (5)
Bulent Gunduz (5)
Nebil Goksu (1)
Ahmet
Arslan (6)
Abdullah Ekmekci (4)
关键词:
hearing loss
;
GJB2 gene
;
connexin 26
刊名:Journal of Genetics
出版年:2008
1
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