Development of distortion product otoacoustic emissions in C57BL/6J mice.
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Hearing loss is an early consequence of Npc1 gene deletion in the mouse model of Niemann-Pick disease, type C.Contralateral ear occlusion for improving the reliability of otoacoustic emission screening tests.Genetic background of Prop1(df) mutants provides remarkable protection against hypothyroidism-induced hearing impairment.Postnatal maturation of contralateral DPOAE suppression in a precocious animal model (chinchilla) of the human neonate.
P2860
Development of distortion product otoacoustic emissions in C57BL/6J mice.
description
2009 nî lūn-bûn
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2009年の論文
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2009年学术文章
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2009年学术文章
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2009年学术文章
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name
Development of distortion product otoacoustic emissions in C57BL/6J mice.
@en
Development of distortion product otoacoustic emissions in C57BL/6J mice.
@nl
type
label
Development of distortion product otoacoustic emissions in C57BL/6J mice.
@en
Development of distortion product otoacoustic emissions in C57BL/6J mice.
@nl
prefLabel
Development of distortion product otoacoustic emissions in C57BL/6J mice.
@en
Development of distortion product otoacoustic emissions in C57BL/6J mice.
@nl
P2093
P2860
P1476
Development of distortion product otoacoustic emissions in C57BL/6J mice.
@en
P2093
Akira Minekawa
Katsuhisa Ikeda
Masayuki Furukawa
Takashi Iizuka
Takeshi Kusunoki
Takuji Koike
Yuya Narui
P2860
P304
P356
10.1080/14992020902858959
P577
2009-08-01T00:00:00Z