TY  - GEN
AU  - Najmabadi,Hossein
AU  - Cucci,Robert A
AU  - Sahebjam,Solmaz
AU  - Kouchakian,Nafiseh
AU  - Farhadi,Mohammad
AU  - Kahrizi,Kimia
AU  - Arzhangi,Sanaz
AU  - Daneshmandan,Naiimeh
AU  - Javan,Khalil
AU  - Smith,Richard J H
TI  - GJB2 mutations in Iranians with autosomal recessive non-syndromic sensorineural hearing loss
SN  - 1098-1004
PY  - 2002///0627
KW  - Connexin 26
KW  - Connexins
KW  - genetics
KW  - Genes, Recessive
KW  - Genetic Carrier Screening
KW  - methods
KW  - Genetic Testing
KW  - Hearing Disorders
KW  - Humans
KW  - Iran
KW  - epidemiology
KW  - Mutation
KW  - Syndrome
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S
UR  - https://doi.org/10.1002/humu.9033
ER  -