Mutations in the connexin26/GJB2 gene are the most common event in non-syndromic hearing loss among the German population

Human mutation

Volumn 17, Issue 6, 2001, Pages 521-522

  Gabriel, Heinz ^a   Kupsch, Petra ^a   Sudendey, Jürgen ^a   Winterhager, Elke ^a   Jahnke, Klaus ^a   Lautermann, Jürgen ^a  

^a UNIVERSITY HOSPITAL ESSEN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

CONNEXIN 26; DNA; GAP JUNCTION PROTEIN;

ADOLESCENT; ADULT; ARTICLE; CHEMISTRY; CHILD; FEMALE; GENETICS; GERMANY; HUMAN; MALE; MIDDLE AGED; MUTATION; NUCLEOTIDE SEQUENCE; PERCEPTION DEAFNESS; PRESCHOOL CHILD;

ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; CONNEXINS; DNA; DNA MUTATIONAL ANALYSIS; FEMALE; GERMANY; HEARING LOSS, SENSORINEURAL; HUMANS; MALE; MIDDLE AGED; MUTATION;

EID: 0035375301     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.1138     Document Type: Article

References (0)