Connexin gene 26 (GJB2) mutations in patients with hereditary non-syndromic sensorineural loss of hearing in the Republic of Sakha (Yakutia)

Vestnik otorinolaringologii

Volumn , Issue 5, 2008, Pages 23-28

  Barashkov, N A ^a   Dzhemileva, L U ^a   Fedorova, S A ^a   Maksimova, N R ^a   Khusnutdinova, E K ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

CONNEXIN 26; DNA; GAP JUNCTION PROTEIN;

ADOLESCENT; ADULT; ARTICLE; CHILD; COMPARATIVE STUDY; FEMALE; GENE FREQUENCY; GENETIC PREDISPOSITION; GENETICS; GENOTYPE; HUMAN; MALE; METABOLISM; MUTATION; PERCEPTION DEAFNESS; PRESCHOOL CHILD; PREVALENCE; RUSSIAN FEDERATION; SINGLE STRAND CONFORMATION POLYMORPHISM;

ADOLESCENT; CHILD; CHILD, PRESCHOOL; CONNEXINS; DNA; FEMALE; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HEARING LOSS, SENSORINEURAL; HUMANS; MALE; MUTATION; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; PREVALENCE; SIBERIA; YOUNG ADULT;

EID: 58149277091     PISSN: 00424668     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)