Low intensities and 1.3 ratio produce distortion product otoacoustic emissions which are larger in heterozygous (+/dn) than homozygous (+/+) mice

Hearing Research

Volumn 117, Issue 1-2, 1998, Pages 24-30

  Huang, Jer Min ^a   Berlin, Charles I ^a   Lin, Shu Tze ^a   Keats, Bronya J B ^a,b  

^a Kresge Hearing Research Laboratory of the South   (United States)

^b LOUISIANA STATE UNIV MEDICAL CENTER   (United States)

Author keywords

Curly tail mouse; Deafness mouse; Distortion product otoacoustic emission; dn gene carrier

Indexed keywords

ANIMAL MODEL; ARTICLE; CHROMOSOME 19; CONTROLLED STUDY; DISTORTION PRODUCT OTOACOUSTIC EMISSION; GENE LOCATION; GENETIC PREDISPOSITION; HEARING IMPAIRMENT; HETEROZYGOTE DETECTION; HOMOZYGOSITY; INNER EAR DISEASE; MARKER GENE; MOUSE; NONHUMAN; PRIORITY JOURNAL; SOUND DETECTION; SOUND INTENSITY;

ACOUSTIC STIMULATION; ANIMALS; DEAFNESS; DISEASE MODELS, ANIMAL; FEMALE; HETEROZYGOTE; HOMOZYGOTE; MALE; MICE; OTOACOUSTIC EMISSIONS, SPONTANEOUS; PHENOTYPE;

EID: 0031896966     PISSN: 03785955     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0378-5955(98)00005-7     Document Type: Article

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