1.
Vestn Otorinolaringol
; (2): 17-9, 2009.
Artigo
em Russo
| MEDLINE
| ID: mdl-19491791
RESUMO
This paper reports the first case of cochlear implantation performed in this country in a child with congenital non-syndromic sensorineural loss of hearing having hereditary etiology and attributable to autosomal-recessive 35 delG mutation in locus DFNB1 (13q.11-q12) of GJB2 (connexin 26) gene.