(Q33881296)

29 July 2017

title

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

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29 July 2017

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Talebizadeh Z

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29 July 2017

Kelley PM

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29 July 2017

Askew JW

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29 July 2017

Beisel KW

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29 July 2017

Smith SD

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29 July 2017

publication date

1 January 1999

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29 July 2017

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29 July 2017

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29 July 2017

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29 July 2017

page(s)

493-501

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Structure and function of voltage-sensitive ion channels

29 July 2017

cites work

1 reference

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A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family

21 January 2018

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Linkage of autosomal dominant hearing loss to the short arm of chromosome 1 in two families

21 January 2018

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

21 January 2018

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Developmental changes in the physiology of hair cells

21 January 2018

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Mitochondrial deafness mutations reviewed

21 January 2018

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Novel mutations in the connexin 26 gene (GJB2) that cause autosomal recessive (DFNB1) hearing loss

21 January 2018

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Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

21 January 2018

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Expression of a potassium current in inner hair cells during development of hearing in mice

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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Strategies for multilocus linkage analysis in humans

21 January 2018

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Distinct expression patterns of notch family receptors and ligands during development of the mammalian inner ear

21 January 2018

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Action potentials and underlying voltage-dependent currents studied in cultured spiral ganglion neurons of the postnatal gerbil

21 January 2018

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Mutations in the myosin VIIA gene cause non-syndromic recessive deafness

21 January 2018

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Nonsyndromic deafness DFNA1 associated with mutation of a human homolog of the Drosophila gene diaphanous

21 January 2018

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Sodium and potassium currents of type I spiral ganglion cells from rat.

21 January 2018

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A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome

21 January 2018

1 reference

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

21 January 2018

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Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channel

21 January 2018

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Divalent cations inhibit IsK/KvLQT1 channels in excised membrane patches of strial marginal cells

21 January 2018

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A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns

21 January 2018

1 reference

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Voltage-activated K channel in luminal membrane of marginal cells of stria vascularis dissected from guinea pig.

21 January 2018

1 reference

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IsK and KvLQT1: mutation in either of the two subunits of the slow component of the delayed rectifier potassium channel can cause Jervell and Lange-Nielsen syndrome

21 January 2018

1 reference

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Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humans

21 January 2018

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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

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Nonsyndromic hearing impairment is associated with a mutation in DFNA5

21 January 2018

1 reference

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Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment

21 January 2018

1 reference

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Ion transport mechanisms responsible for K+ secretion and the transepithelial voltage across marginal cells of stria vascularis in vitro

21 January 2018

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Mutations in the gene encoding gap junction protein beta-3 associated with autosomal dominant hearing impairment

21 January 2018

1 reference

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Patch clamped responses from outer hair cells in the intact adult organ of Corti

21 January 2018

1 reference

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Making a submicroscopic hole in one

21 January 2018

1 reference

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10.1002/(SICI)1098-1004(199912)14:6<493::AID-HUMU8>3.0.CO;2-P

21 January 2018

Identifiers

DOI

1 reference

29 July 2017

1 reference