Mapping and characterization of a novel cochlear gene in human and in mouse: A positional candidate gene for a deafness disorder, DFNA9

Genomics

Volumn 46, Issue 3, 1997, Pages 345-354

  Robertson, Nahid G ^a   Skvorak, Anne B ^a,c   Yin, Yi ^a,c   Weremowicz, Stanislawa ^a,c   Johnson, Kenneth R ^d   Kovatch, Kristina A ^a   Battey, James F ^e   Bieber, Frederick R ^a,c   Morton, Cynthia C ^a,b,c  

^a Department of Pathology ^*  (United States)

^b BRIGHAM AND WOMEN S HOSPITAL   (United States)

^c HARVARD MEDICAL SCHOOL   (United States)

^d JACKSON LABORATORY   (United States)

^e NATIONAL INSTITUTE ON DEAFNESS AND OTHER COMMUNICATION DISORDERS   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

VON WILLEBRAND FACTOR;

ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHROMOSOME 12; CHROMOSOME 14Q; DNA TRANSCRIPTION; EXTRACELLULAR MATRIX; GENE ACTIVITY; GENE EXPRESSION; GENE ISOLATION; GENE LOCUS; GENE MAPPING; GENETIC DISORDER; HEARING IMPAIRMENT; HUMAN; HYBRIDIZATION; MARKER GENE; NONHUMAN; NORTHERN BLOTTING; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; SEQUENCE HOMOLOGY;

EID: 0031573922     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1997.5067     Document Type: Article

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