GJB2 mutations in Iranians with autosomal recessive non-syndromic sensorineural hearing loss.

Human mutation

Volumn 19, Issue 5, 2002, Pages 572-

  Najmabadi, Hossein ^a   Cucci, Robert A ^a   Sahebjam, Solmaz ^a   Kouchakian, Nafiseh ^a   Farhadi, Mohammad ^a   Kahrizi, Kimia ^a   Arzhangi, Sanaz ^a   Daneshmandan, Naiimeh ^a   Javan, Khalil ^a   Smith, Richard J H ^a  

^a UNIVERSITY OF SOCIAL WELFARE AND REHABILITATION SCIENCES   (Iran)

Author keywords

[No Author keywords available]

Indexed keywords

CONNEXIN 26; GAP JUNCTION PROTEIN;

ARTICLE; GENETIC SCREENING; GENETICS; HEARING DISORDER; HETEROZYGOTE DETECTION; HUMAN; IRAN; METHODOLOGY; MUTATION; RECESSIVE GENE; SYNDROME;

CONNEXINS; GENES, RECESSIVE; GENETIC SCREENING; HEARING DISORDERS; HETEROZYGOTE DETECTION; HUMANS; IRAN; MUTATION; SYNDROME;

EID: 0036580878     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.9033     Document Type: Article

References (0)