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Connexin 26 mutations in hereditary non-syndromic sensorineural deafness
scientific journal article
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Statements
instance of
scholarly article
1 reference
stated in
PubMed
PubMed ID
9139825
retrieved
4 January 2017
title
Connexin 26 mutations in hereditary non-syndromic sensorineural deafness
(English)
1 reference
stated in
PubMed
PubMed ID
9139825
retrieved
4 January 2017
main subject
deafness
1 reference
based on heuristic
inferred from title
author
David P. Kelsell
0 references
author name string
D. P. Kelsell
series ordinal
1
1 reference
stated in
PubMed
PubMed ID
9139825
retrieved
4 January 2017
J. Dunlop
series ordinal
2
1 reference
stated in
PubMed
PubMed ID
9139825
retrieved
4 January 2017
H. P. Stevens
series ordinal
3
1 reference
stated in
PubMed
PubMed ID
9139825
retrieved
4 January 2017
N. J. Lench
series ordinal
4
1 reference
stated in
PubMed
PubMed ID
9139825
retrieved
4 January 2017
J. N. Liang
series ordinal
5
1 reference
stated in
PubMed
PubMed ID
9139825
retrieved
4 January 2017
G. Parry
series ordinal
6
1 reference
stated in
PubMed
PubMed ID
9139825
retrieved
4 January 2017
R. F. Mueller
series ordinal
7
1 reference
stated in
PubMed
PubMed ID
9139825
retrieved
4 January 2017
I. M. Leigh
series ordinal
8
1 reference
stated in
PubMed
PubMed ID
9139825
retrieved
4 January 2017
language of work or name
English
0 references
publication date
1 May 1997
1 reference
stated in
PubMed
PubMed ID
9139825
retrieved
4 January 2017
published in
Nature
1 reference
stated in
PubMed
PubMed ID
9139825
retrieved
4 January 2017
volume
387
1 reference
stated in
PubMed
PubMed ID
9139825
retrieved
4 January 2017
issue
6628
1 reference
stated in
PubMed
PubMed ID
9139825
retrieved
4 January 2017
page(s)
80–83
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stated in
PubMed
PubMed ID
9139825
retrieved
4 January 2017
cites work
Genetic epidemiology of hearing impairment
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F387080A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F387080A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the PAX3 gene causing Waardenburg syndrome type 1 and type 2
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F387080A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Defective myosin VIIA gene responsible for Usher syndrome type 1B
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F387080A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hereditary palmoplantar keratoderma with deafness
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F387080A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A human gene responsible for neurosensory, non-syndromic recessive deafness is a candidate homologue of the mouse sh-1 gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F387080A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A gene responsible for a dominant form of neurosensory non-syndromic deafness maps to the NSRD1 recessive deafness gene interval
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F387080A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The gene responsible for Clouston hidrotic ectodermal dysplasia maps to the pericentromeric region of chromosome 13q
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F387080A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Assignment of connexin 26 (GJB2) and 46 (GJA3) genes to human chromosome 13q11-->q12 and mouse chromosome 14D1-E1 by in situ hybridization
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F387080A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The gap junction communication channel
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F387080A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular biology and genetics of gap junction channels
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F387080A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Expression of gap junction proteins Cx26, Cx31.1, Cx37, and Cx43 in developing and mature rat epidermis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F387080A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Structure of gap junction intercellular channels
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F387080A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Keratin expression in basal cell carcinomas
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F387080A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genes responsible for human hereditary deafness: symphony of a thousand
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F387080A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Connexin mutations in X-linked Charcot-Marie-Tooth disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F387080A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations of the Connexin43 gap-junction gene in patients with heart malformations and defects of laterality
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F387080A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/387080A0
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1289966
Dimensions Publication ID
1017615074
0 references
OpenCitations bibliographic resource ID
1289966
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1289966
PubMed ID
9139825
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1289966
ResearchGate publication ID
14078257
0 references
Springer Nature article ID
10.1038/387080a0
0 references
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