Phenotype and genetics of progressive sensorineural hearing loss (Snhl1) in the LXS set of recombinant inbred strains of mice

PLoS ONE

Volumn 5, Issue 7, 2010, Pages

  Noben Trauth, Konrad ^a   Latoche, Joseph R ^a   Neely, Harold R ^a   Bennett, Beth ^b  

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

^b UNIVERSITY OF COLORADO   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GENE PRODUCT; SENSORINEURAL HEARING LOSS 1 PROTEIN; UNCLASSIFIED DRUG;

AGE; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CHROMOSOMAL LOCALIZATION; CHROMOSOME 10; COCHLEA POTENTIAL; CONTROLLED STUDY; EVOKED BRAIN STEM AUDITORY RESPONSE; GENE LOCUS; GENE MAPPING; GENETIC VARIABILITY; HISTOPATHOLOGY; INNER EAR; MOUSE; MOUSE STRAIN; NONHUMAN; OTOACOUSTIC EMISSION; PATHOGENESIS; PERCEPTION DEAFNESS; PHENOTYPIC VARIATION; STRAIN DIFFERENCE; ANIMAL; COCHLEA; EVOKED AUDITORY RESPONSE; GENETICS; GENOTYPE; HUMAN; METABOLISM; PHENOTYPE; QUANTITATIVE TRAIT LOCUS; REGRESSION ANALYSIS;

MUS;

ANIMALS; CHROMOSOMES, HUMAN, PAIR 10; COCHLEA; EAR, INNER; EVOKED POTENTIALS, AUDITORY; GENOTYPE; HEARING LOSS, SENSORINEURAL; HUMANS; MICE; PHENOTYPE; QUANTITATIVE TRAIT LOCI; REGRESSION ANALYSIS;

EID: 77955384851     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0011459     Document Type: Article

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