Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction (Q28117054)

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4 January 2017

S. Heller

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4 January 2017

S. N. Merchant

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4 January 2017

R. D. Eavey

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4 January 2017

M. McKenna

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4 January 2017

J. B. Nadol

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4 January 2017

R. T. Miyamoto

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4 January 2017

F. H. Linthicum

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4 January 2017

J. F. Lubianca Neto

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4 January 2017

A. J. Hudspeth

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4 January 2017

C. E. Seidman

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4 January 2017

C. C. Morton

Genes responsible for human hereditary deafness: symphony of a thousand

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4 January 2017

language of work or name

English

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publication date

1 November 1998

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4 January 2017

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4 January 2017

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299–303

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4 January 2017

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7 January 2021

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

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7 January 2021

The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene

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7 January 2021

Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA gene

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7 January 2021

Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3.

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7 January 2021

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

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7 January 2021

Connexin mutations and hearing loss.

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7 January 2021

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

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7 January 2021

Connexin 26 gene linked to a dominant deafness.

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7 January 2021

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

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7 January 2021

A mutation in PDS causes non-syndromic recessive deafness

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Isolation of novel and known genes from a human fetal cochlear cDNA library using subtractive hybridization and differential screening

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Autosomal dominant sensorineural hearing loss. Further temporal bone findings

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7 January 2021

Type A modules: interacting domains found in several non-fibrillar collagens and in other extracellular matrix proteins

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7 January 2021

Basic local alignment search tool

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7 January 2021

Molecular mechanism of hemolymph clotting system in Limulus

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7 January 2021

Intracellular serine-protease zymogen, factor C, from horseshoe crab hemocytes. Its activation by synthetic lipid A analogues and acidic phospholipids

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7 January 2021

A single protocol to detect transcripts of various types and expression levels in neural tissue and cultured cells: in situ hybridization using digoxigenin-labelled cRNA probes

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7 January 2021

Missense mutation in the pore region of HERG causes familial long QT syndrome

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7 January 2021