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English
Connexins, hearing and deafness: clinical aspects of mutations in the connexin 26 gene
scientific article published on 01 April 2000
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10928803
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10928803%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
review article
1 reference
stated in
Europe PubMed Central
title
Connexins, hearing and deafness: clinical aspects of mutations in the connexin 26 gene
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10928803
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10928803%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
author name string
P P Lefebvre
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10928803
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10928803%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
T R Van De Water
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10928803
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10928803%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
publication date
1 April 2000
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10928803
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10928803%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
volume
32
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10928803
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10928803%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
issue
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10928803
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10928803%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
page(s)
159-162
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10928803
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10928803%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
cites work
Genetic epidemiology of hearing impairment
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900075-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900075-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Two different connexin 26 mutations in an inbred kindred segregating non-syndromic recessive deafness: implications for genetic studies in isolated populations.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900075-2
retrieved
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900075-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the connexin 26 gene (GJB2) among Ashkenazi Jews with nonsyndromic recessive deafness
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900075-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Connexin 26 gene linked to a dominant deafness
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900075-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Connexin mutations and hearing loss.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900075-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Multiple connexin proteins in single intercellular channels: connexin compatibility and functional consequences
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900075-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Connexin 26 mutations in hereditary non-syndromic sensorineural deafness
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900075-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Gap junctions in the rat cochlea: immunohistochemical and ultrastructural analysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900075-2
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/10.1016%2FS0165-0173%2899%2900075-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Functional defects of Cx26 resulting from a heterozygous missense mutation in a family with dominant deaf-mutism and palmoplantar keratoderma.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900075-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Stimulated acoustic emissions from within the human auditory system
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900075-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Evoked mechanical responses of isolated cochlear outer hair cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900075-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0165-0173(99)00075-2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10928803
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10928803%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
PubMed publication ID
10928803
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10928803
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10928803%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
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