Deafness and mutations in the connexin 26 gene [2] (multiple letters)

New England Journal of Medicine

Volumn 340, Issue 16, 1999, Pages 1288-

  Zlotogora, J ^a   Morell, R J ^a   Friedman, T B ^a  

^a HEBREW UNIVERSITY   (Israel)

Author keywords

[No Author keywords available]

Indexed keywords

GAP JUNCTION PROTEIN;

DIAGNOSTIC APPROACH ROUTE; FREQUENCY ANALYSIS; GENE MUTATION; HEARING IMPAIRMENT; HETEROZYGOTE; HUMAN; HUMAN CELL; HUMAN TISSUE; HYPOTHYROIDISM; JEW; LETTER; PHENYLKETONURIA; PRIORITY JOURNAL;

CONNEXINS; DEAFNESS; GENETIC SCREENING; HEARING TESTS; HUMANS; JEWS; MASS SCREENING;

EID: 0033594382     PISSN: 00284793     EISSN: None     Source Type: Journal    
DOI: 10.1056/NEJM199904223401614     Document Type: Letter

References (0)