Pattern of connexin 26 (GJB2) mutations causing sensorineural hearing impairment in Ghana

Human mutation

Volumn 18, Issue 1, 2001, Pages 84-85

  Hamelmann, Christoph ^a   Amedofu, Geoffrey K ^b   Albrecht, Katrin ^a   Muntau, Birgit ^a   Gelhaus, Annette ^a   Brobby, George W ^b   Horstmann, Rolf D ^a  

^a BERNHARD NOCHT INSTITUTE FOR TROPICAL MEDICINE   (Germany)

^b KWAME NKRUMAH UNIVERSITY OF SCIENCE AND TECHNOLOGY   (Ghana)

Author keywords

[No Author keywords available]

Indexed keywords

CONNEXIN 26; GAP JUNCTION PROTEIN;

ADOLESCENT; ADULT; ARTICLE; CHEMISTRY; CHILD; DOMINANT GENE; GENETIC SCREENING; GENETICS; GENOTYPE; GHANA; HUMAN; MISSENSE MUTATION; MUTATION; PERCEPTION DEAFNESS; RECESSIVE GENE;

ADOLESCENT; ADULT; CHILD; CONNEXINS; GENES, DOMINANT; GENES, RECESSIVE; GENETIC SCREENING; GENOTYPE; GHANA; HEARING LOSS, SENSORINEURAL; HUMANS; MUTATION; MUTATION, MISSENSE;

EID: 0035232752     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.1156     Document Type: Article

References (0)