GJB2 mutations in Iranians with autosomal recessive non-syndromic sensorineural hearing loss.
Najmabadi, Hossein
GJB2 mutations in Iranians with autosomal recessive non-syndromic sensorineural hearing loss. [electronic resource] - Human mutation May 2002 - 572 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
1098-1004
10.1002/humu.9033 doi
Connexin 26
Connexins--genetics
Genes, Recessive--genetics
Genetic Carrier Screening--methods
Genetic Testing--methods
Hearing Disorders--genetics
Humans
Iran--epidemiology
Mutation--genetics
Syndrome
GJB2 mutations in Iranians with autosomal recessive non-syndromic sensorineural hearing loss. [electronic resource] - Human mutation May 2002 - 572 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
1098-1004
10.1002/humu.9033 doi
Connexin 26
Connexins--genetics
Genes, Recessive--genetics
Genetic Carrier Screening--methods
Genetic Testing--methods
Hearing Disorders--genetics
Humans
Iran--epidemiology
Mutation--genetics
Syndrome