A mutational hot spot in the KCNQ4 gene responsible for autosomal dominant hearing impairment (Q34138254)

31 July 2017

A mutational hot spot in the KCNQ4 gene responsible for autosomal dominant hearing impairment (English)

1 reference

31 July 2017

1 reference

9

Shin-Ichi Usami

1 reference

31 July 2017

8

Cor W R J Cremers

1 reference

31 July 2017

Guy Van Camp

1

1 reference

31 July 2017

Paul J Coucke

2

1 reference

31 July 2017

Jiro Akita

3

1 reference

31 July 2017

Erik Fransen

4

1 reference

31 July 2017

Satoko Abe

5

1 reference

31 July 2017

Els M R De Leenheer

6

1 reference

31 July 2017

Patrick L M Huygen

7

1 reference

31 July 2017

language of work or name

1 reference

1 July 2002

1 reference

31 July 2017

1 reference

31 July 2017

20

1 reference

31 July 2017

15-19

1 reference

31 July 2017

1

1 reference

A fast and scalable radiation hybrid map construction and integration strategy

31 July 2017

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10096

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10096

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10096

The Structure of the Potassium Channel: Molecular Basis of K+ Conduction and Selectivity

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10096

A Dutch family with progressive sensorineural hearing impairment linked to the DFNA2 region.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10096

Connexin-26 mutations in sporadic and inherited sensorineural deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10096

Automobile crashes and teenaged drivers

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10096

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10096

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10096

Nonsyndromic autosomal dominant progressive sensorineural hearing loss: audiologic analysis of a pedigree linked to DFNA2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10096

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/10.1002%2FHUMU.10096

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10096

Linkage analysis of progressive hearing loss in five extended families maps the DFNA2 gene to a 1.25-Mb region on chromosome 1p

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10096

Mutations in the KCNQ4 K+ channel gene, responsible for autosomal dominant hearing loss, cluster in the channel pore region.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10096

Mutations in fibroblast growth-factor receptor 3 in sporadic cases of achondroplasia occur exclusively on the paternally derived chromosome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10096

21 January 2018

Identifiers

DOI

10.1002/HUMU.10096

1 reference

31 July 2017

1 reference