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English
Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction
scientific journal article
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scholarly article
1 reference
stated in
PubMed
PubMed ID
9806553
retrieved
4 January 2017
title
Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction
(English)
1 reference
stated in
PubMed
PubMed ID
9806553
retrieved
4 January 2017
main subject
nonsyndromic deafness
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based on heuristic
inferred from title
vestibular disease
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inferred from title
deafness
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inferred from title
author
Jonathan G Seidman
series ordinal
14
object named as
J. G. Seidman
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PubMed
PubMed ID
9806553
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4 January 2017
author name string
N. G. Robertson
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1
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PubMed
PubMed ID
9806553
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4 January 2017
L. Lu
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2
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PubMed
PubMed ID
9806553
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S. Heller
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3
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PubMed
PubMed ID
9806553
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S. N. Merchant
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PubMed
PubMed ID
9806553
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R. D. Eavey
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PubMed ID
9806553
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M. McKenna
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6
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PubMed
PubMed ID
9806553
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J. B. Nadol
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PubMed ID
9806553
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R. T. Miyamoto
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9806553
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F. H. Linthicum
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PubMed
PubMed ID
9806553
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J. F. Lubianca Neto
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PubMed
PubMed ID
9806553
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A. J. Hudspeth
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PubMed
PubMed ID
9806553
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C. E. Seidman
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12
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PubMed
PubMed ID
9806553
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C. C. Morton
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13
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PubMed
PubMed ID
9806553
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4 January 2017
language of work or name
English
0 references
publication date
1 November 1998
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PubMed
PubMed ID
9806553
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4 January 2017
published in
Nature Genetics
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PubMed
PubMed ID
9806553
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4 January 2017
volume
20
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PubMed
PubMed ID
9806553
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4 January 2017
page(s)
299–303
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PubMed
PubMed ID
9806553
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issue
3
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PubMed
PubMed ID
9806553
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4 January 2017
cites work
Genes responsible for human hereditary deafness: symphony of a thousand
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F3118
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the myosin VIIA gene cause non-syndromic recessive deafness
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F3118
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7 January 2021
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inferred from DOI database lookup
The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F3118
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7 January 2021
based on heuristic
inferred from DOI database lookup
Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA gene
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reference URL
https://api.crossref.org/works/10.1038%2F3118
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7 January 2021
based on heuristic
inferred from DOI database lookup
Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F3118
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7 January 2021
based on heuristic
inferred from DOI database lookup
Connexin 26 mutations in hereditary non-syndromic sensorineural deafness
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F3118
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Connexin mutations and hearing loss.
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F3118
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7 January 2021
based on heuristic
inferred from DOI database lookup
Novel mutations in the connexin 26 gene (GJB2) that cause autosomal recessive (DFNB1) hearing loss
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F3118
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7 January 2021
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inferred from DOI database lookup
Connexin 26 gene linked to a dominant deafness.
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reference URL
https://api.crossref.org/works/10.1038%2F3118
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7 January 2021
based on heuristic
inferred from DOI database lookup
Nonsyndromic deafness DFNA1 associated with mutation of a human homolog of the Drosophila gene diaphanous
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reference URL
https://api.crossref.org/works/10.1038%2F3118
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7 January 2021
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A mutation in PDS causes non-syndromic recessive deafness
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F3118
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7 January 2021
based on heuristic
inferred from DOI database lookup
Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humans
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F3118
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7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F3118
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7 January 2021
based on heuristic
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Isolation of novel and known genes from a human fetal cochlear cDNA library using subtractive hybridization and differential screening
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F3118
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mapping and characterization of a novel cochlear gene in human and in mouse: a positional candidate gene for a deafness disorder, DFNA9
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F3118
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7 January 2021
based on heuristic
inferred from DOI database lookup
A gene for non-syndromic autosomal dominant progressive postlingual sensorineural hearing loss maps to chromosome 14q12-13
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F3118
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7 January 2021
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inferred from DOI database lookup
Autosomal dominant sensorineural hearing loss. Pedigrees, audiologic findings, and temporal bone findings in two kindreds
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F3118
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7 January 2021
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inferred from DOI database lookup
Autosomal dominant sensorineural hearing loss. Further temporal bone findings
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reference URL
https://api.crossref.org/works/10.1038%2F3118
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7 January 2021
based on heuristic
inferred from DOI database lookup
Type A modules: interacting domains found in several non-fibrillar collagens and in other extracellular matrix proteins
1 reference
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https://api.crossref.org/works/10.1038%2F3118
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7 January 2021
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Basic local alignment search tool
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https://api.crossref.org/works/10.1038%2F3118
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7 January 2021
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inferred from DOI database lookup
Molecular mechanism of hemolymph clotting system in Limulus
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https://api.crossref.org/works/10.1038%2F3118
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Intracellular serine-protease zymogen, factor C, from horseshoe crab hemocytes. Its activation by synthetic lipid A analogues and acidic phospholipids
1 reference
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reference URL
https://api.crossref.org/works/10.1038%2F3118
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7 January 2021
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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
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F3118
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7 January 2021
based on heuristic
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Missense mutation in the pore region of HERG causes familial long QT syndrome
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F3118
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7 January 2021
based on heuristic
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Identifiers
DOI
10.1038/3118
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
2286139
OpenCitations bibliographic resource ID
2286139
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
2286139
PubMed ID
9806553
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
2286139
ResearchGate publication ID
13479096
0 references
Springer Nature article ID
10.1038/3118
0 references
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