Connexin 26 R143W mutation associated with recessive nonsyndromic sensorineural deafness in Africa [4]

New England Journal of Medicine

Volumn 338, Issue 8, 1998, Pages 548-550

  Brobby, G W ^a   Muller Myhsok, B ^a   Horstmann, R D ^a  

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

Author keywords

[No Author keywords available]

Indexed keywords

GAP JUNCTION PROTEIN;

AMINO ACID SUBSTITUTION; AUDIOMETRY; CHROMOSOME 13Q; CLINICAL ARTICLE; DISEASE ASSOCIATION; DOMINANT INHERITANCE; GENE MUTATION; GENE SEQUENCE; HEARING IMPAIRMENT; HUMAN; LETTER; PERCEPTION DEAFNESS; PRIORITY JOURNAL; RECESSIVE INHERITANCE;

EID: 0032546033     PISSN: 00284793     EISSN: None     Source Type: Journal    
DOI: 10.1056/NEJM199802193380813     Document Type: Letter

References (5)