Hearing loss in the RBF/DnJ mouse, a proposed animal model of Usher syndrome type IIa

Hearing Research

Volumn 112, Issue 1-2, 1997, Pages 1-12

  Pieke Dahl, Sandra ^a   Ohlemiller, Kevin K ^b   McGee, JoAnn ^a   Walsh, Edward J ^a   Kimberling, William J ^a  

^a BOYS TOWN NATIONAL RESEARCH HOSPITAL   (United States)

^b CENTRAL INSTITUTE FOR THE DEAF   (United States)

Author keywords

RBF DnJ; rd3; USH2A; Usher syndrome type IIa

Indexed keywords

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; AUDIOLOGY; AUTOSOMAL RECESSIVE DISORDER; CHROMOSOME 1Q; CONTROLLED STUDY; DNA FLANKING REGION; FEMALE; GENOTYPE; HAPLOTYPE; HEARING LOSS; INBRED STRAIN; MALE; MOUSE; NONHUMAN; PERCEPTION DEAFNESS; PRIORITY JOURNAL; PROGENY; RECESSIVE GENE; RETINA DEGENERATION; RETINITIS PIGMENTOSA; USHER SYNDROME;

ANIMALS; CHROMOSOME MAPPING; COCHLEA; DISEASE MODELS, ANIMAL; EVOKED POTENTIALS, AUDITORY, BRAIN STEM; GENES, RECESSIVE; HEARING LOSS, SENSORINEURAL; HUMANS; LINKAGE (GENETICS); MICE; MICE, MUTANT STRAINS; PHENOTYPE; RETINA; RETINITIS PIGMENTOSA; SYNDROME;

EID: 0030769184     PISSN: 03785955     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0378-5955(97)00087-7     Document Type: Article

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