(Q50488834)

14 March 2018

title

Hereditary cochleovestibular dysfunction due to a COCH gene mutation (DFNA9): a follow-up study of a family (English)

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14 March 2018

author name string

Verhagen WI

1

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14 March 2018

Bom SJ

2

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14 March 2018

Fransen E

3

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14 March 2018

Van Camp G

4

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14 March 2018

Huygen PL

5

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14 March 2018

Theunissen EJ

6

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14 March 2018

Cremers CW

7

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14 March 2018

publication date

1 December 2001

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14 March 2018

published in

Clinical Otolaryngology

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14 March 2018

volume

26

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14 March 2018

issue

6

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14 March 2018

page(s)

477-483

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14 March 2018

Non-syndromal autosomal dominant hearing impairment: ongoing phenotypical characterization of genotypes

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Autosomal dominant sensorineural hearing loss. Pedigrees, audiologic findings, and temporal bone findings in two kindreds

21 January 2018

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Autosomal dominant sensorineural hearing loss. Further temporal bone findings

21 January 2018

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A gene for non-syndromic autosomal dominant progressive postlingual sensorineural hearing loss maps to chromosome 14q12-13

21 January 2018

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High prevalence of symptoms of Menière's disease in three families with a mutation in the COCH gene

21 January 2018

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A Pro51Ser mutation in the COCH gene is associated with late onset autosomal dominant progressive sensorineural hearing loss with vestibular defects

21 January 2018

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Mapping and characterization of a novel cochlear gene in human and in mouse: a positional candidate gene for a deafness disorder, DFNA9

21 January 2018

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https://api.crossref.org/works/10.1046%2FJ.1365-2273.2001.00505.X

Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction

21 January 2018

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A common ancestor for COCH related cochleovestibular (DFNA9) patients in Belgium and The Netherlands bearing the P51S mutation.

21 January 2018

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Familial progressive vestibulocochlear dysfunction

21 January 2018

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Hereditary vestibulo-cochlear dysfunction and vascular disorders

21 January 2018

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A new autosomal dominant syndrome of idiopathic progressive vestibulo-cochlear dysfunction with middle-age onset

21 January 2018

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Progressive cochleovestibular impairment caused by a point mutation in the COCH gene at DFNA9.

21 January 2018

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Familial progressive vestibulocochlear dysfunction caused by a COCH mutation (DFNA9).

21 January 2018

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Oculomotor, auditory, and vestibular responses in myotonic dystrophy

21 January 2018

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Diagnostic value of velocity-step responses

21 January 2018

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Single-response variability of air and water caloric reactions

21 January 2018

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Histopathology of the inner ear in DFNA9.

21 January 2018

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DFNA9 is a progressive audiovestibular dysfunction with a microfibrillar deposit in the inner ear.

21 January 2018

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21 January 2018

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Identification of the protein product of the Coch gene (hereditary deafness gene) as the major component of bovine inner ear protein

21 January 2018

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21 January 2018

Identifiers

DOI

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14 March 2018

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14 March 2018