(Q48595793)

13 February 2018

title

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

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13 February 2018

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Pieke-Dahl S

1

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13 February 2018

Ohlemiller KK

2

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13 February 2018

McGee J

3

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13 February 2018

Walsh EJ

4

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13 February 2018

Kimberling WJ

5

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13 February 2018

publication date

1 October 1997

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13 February 2018

published in

Hearing Research

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13 February 2018

volume

112

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13 February 2018

page(s)

1-12

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13 February 2018

issue

1-2

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13 February 2018

New mouse primary retinal degeneration (rd-3)

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Molecular genetics of retinitis pigmentosa

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Genetic expression of cyclic GMP phosphodiesterase activity defines abnormal photoreceptor differentiation in neurological mutants of inherited retinal degeneration

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7 January 2021

A type VII myosin encoded by the mouse deafness gene shaker-1

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7 January 2021

Screening for mouse retinal degenerations. I. Correlation of indirect ophthalmoscopy, electroretinograms, and histology

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7 January 2021

Digenic retinitis pigmentosa due to mutations at the unlinked peripherin/RDS and ROM1 loci

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7 January 2021

Maps of linkage and synteny homologies between mouse and man.

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7 January 2021

Comparative gene mapping, genome duplication, and the genetics of hearing

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Polygenic disease and retinitis pigmentosa: albinism exacerbates photoreceptor degeneration induced by the expression of a mutant opsin in transgenic mice

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7 January 2021

Inherited hearing defects in mice

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7 January 2021

The construction of a yeast artificial chromosome (YAC) contig in the vicinity of the Usher syndrome type IIa (USH2A) gene in 1q41.

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The endolymphatic sac and inner ear homeostasis. II: Effect of glycerol on the sensory end organs with or without colchicine pretreatment.

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Defective myosin VIIA gene responsible for Usher syndrome type 1B

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10.1016/S0378-5955(97)00087-7

Identifiers

DOI

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13 February 2018

PubMed ID

9367224

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13 February 2018