(Q30955016)

27 June 2017

title

Usher syndrome type III can mimic other types of Usher syndrome (English)

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27 June 2017

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6

Cor W R J Cremers

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27 June 2017

Ronald J E Pennings

1

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27 June 2017

Randall R Fields

2

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27 June 2017

Patrick L M Huygen

3

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27 June 2017

August F Deutman

4

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27 June 2017

William J Kimberling

5

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27 June 2017

publication date

1 June 2003

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Annals of Otology Rhinology and Laryngology

27 June 2017

number of pages

6

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based on heuristic

inferred from page(s)

published in

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27 June 2017

volume

112

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27 June 2017

issue

6

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27 June 2017

page(s)

525-530

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Progressive hearing loss in Usher's syndrome.

27 June 2017

cites work

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https://api.crossref.org/works/10.1177%2F000348940311200608

Usher's syndrome type 3 in Finland.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348940311200608

The ophthalmological course of Usher syndrome type III.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348940311200608

Mutations in a novel gene with transmembrane domains underlie Usher syndrome type 3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348940311200608

Refined mapping of the Usher syndrome type III locus on chromosome 3, exclusion of candidate genes, and identification of the putative mouse homologous region

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348940311200608

A sequence-ready map of the Usher syndrome type III critical region on chromosome 3q

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348940311200608

Assignment of an Usher syndrome type III (USH3) gene to chromosome 3q.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348940311200608

Usher syndrome type III: revised genomic structure of the USH3 gene and identification of novel mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348940311200608

USH3A transcripts encode clarin-1, a four-transmembrane-domain protein with a possible role in sensory synapses

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348940311200608

Inherited nonsyndromic hearing loss. An audiovestibular study in a large family with autosomal dominant progressive hearing loss related to DFNA2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348940311200608

Cervico-ocular reflex enhancement in labyrinthine-defective and normal subjects

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348940311200608

Usher syndrome type III (USH3) linked to chromosome 3q in an Italian family

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348940311200608

Pure tone hearing thresholds and speech recognition scores in Dutch patients carrying mutations in the USH2A gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348940311200608

A new clinical classification for Usher's syndrome based on a new subtype of Usher's syndrome type I.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348940311200608

Ophthalmologic findings in Usher syndrome type 2A.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348940311200608

Familial occurrence of retinitis punctata albescens and congenital sensorineural deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348940311200608

10.1177/000348940311200608

21 January 2018

Identifiers

DOI

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27 June 2017

1 reference