(Q30357338)

20 June 2017

title

Identification of novel mutations in the KCNQ4 gene of patients with nonsyndromic deafness from Taiwan. (English)

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20 June 2017

main subject

nonsyndromic deafness

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Ching-Chyuan Su

1

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20 June 2017

Jiann-Jou Yang

2

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20 June 2017

Jia-Ching Shieh

3

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20 June 2017

Mao-Chang Su

4

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20 June 2017

Shuan-Yow Li

5

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20 June 2017

publication date

10 October 2006

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Audiology and Neuro-Otology

20 June 2017

published in

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20 June 2017

volume

12

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20 June 2017

issue

1

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20 June 2017

page(s)

20-26

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Longitudinal gradients of KCNQ4 expression in spiral ganglion and cochlear hair cells correlate with progressive hearing loss in DFNA2.

20 June 2017

cites work

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Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 families.

21 January 2018

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KCNQ4, a K+ channel mutated in a form of dominant deafness, is expressed in the inner ear and the central auditory pathway.

21 January 2018

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KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness

21 January 2018

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Moderate loss of function of cyclic-AMP-modulated KCNQ2/KCNQ3 K+ channels causes epilepsy

21 January 2018

1 reference

Novel mutation in the KCNQ4 gene in a large kindred with dominant progressive hearing loss

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1159/000096154

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20 June 2017

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