Nonsyndromic hearing impairment is associated with a mutation in DFNA5

Nature Genetics

Volumn 20, Issue 2, 1998, Pages 194-197

  Van Laer, Lut ^a   Huizing, Egbert H ^b   Verstreken, Margriet ^a   Van Zuijlen, Diederick ^b   Wauters, Jan G ^a   Bossuyt, Paul J ^a   Van Heyning, Paul De ^a   McGuirt, Wyman T ^c   Smith, Richard J H ^c   Willems, Patrick J ^a   Kevin Legan, P ^d   Richardson, Guy P ^d   Van Camp, Guy ^a  

^a UNIVERSITY OF ANTWERP   (Belgium)

^b UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

^c UNIVERSITY OF IOWA HOSPITALS AND CLINICS   (United States)

^d UNIVERSITY OF SUSSEX   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CALCULATION; CHROMOSOME 7; EXON; GENE MAPPING; GENE SEQUENCE; GENOME; HEARING IMPAIRMENT; HEREDITY; HUMAN; INTRON; NUCLEOTIDE SEQUENCE; OPEN READING FRAME; PRIORITY JOURNAL; SEGREGATION ANALYSIS;

ADOLESCENT; AMINO ACID SEQUENCE; ANIMALS; CARRIER PROTEINS; CHILD; CHILD, PRESCHOOL; CHROMOSOME MAPPING; FEMALE; HEARING LOSS, HIGH-FREQUENCY; HUMANS; LINKAGE (GENETICS); MALE; MICE; MOLECULAR SEQUENCE DATA; MUTATION; OPEN READING FRAMES; PEDIGREE; PRESBYCUSIS; RECEPTORS, ESTROGEN; SEQUENCE ALIGNMENT;

EID: 17344371515     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/2503     Document Type: Article

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