GJB2 and mitochondrial A1555G gene mutations in nonsyndromic profound hearing loss and carrier frequencies in healthy individuals.

Baysal, Elif; Bayazit, Yildirim A; Ceylaner, Serdar; Alatas, Necat; Donmez, Buket; Ceylaner, Gulay; San, Imran; Korkmaz, Baki; Yilmaz, Akin; Menevse, Adnan; Altunyay, Senay; Gunduz, Bulent; Goksu, Nebil; Arslan, Ahmet; Ekmekci, Abdullah.
J Genet ; 2008 Apr; 87(1): 53-7
Artículo en Inglés | IMSEAR | ID: sea-114368

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