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English
Connexin-26 mutations in sporadic non-syndromal sensorineural deafness
scientific article published on 01 February 1998
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9482297
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9482297%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
title
Connexin-26 mutations in sporadic non-syndromal sensorineural deafness
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9482297
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9482297%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
main subject
deafness
1 reference
based on heuristic
inferred from title
author
Nicholas Lench
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9482297
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9482297%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
Guy Van Camp
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9482297
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9482297%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
author name string
M Houseman
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9482297
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9482297%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
V Newton
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9482297
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9482297%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
R Mueller
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9482297
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9482297%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
language of work or name
English
0 references
publication date
1 February 1998
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9482297
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9482297%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
published in
The Lancet
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9482297
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9482297%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
volume
351
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9482297
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9482297%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
issue
9100
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9482297
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9482297%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
page(s)
415
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9482297
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9482297%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
cites work
Connexin 26 mutations in hereditary non-syndromic sensorineural deafness
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2898%2924006-2
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%2FS0140-6736%2898%2924006-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2898%2924006-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Digenic retinitis pigmentosa due to mutations at the unlinked peripherin/RDS and ROM1 loci
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2898%2924006-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0140-6736(98)24006-2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9482297
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9482297%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
PubMed publication ID
9482297
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9482297
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9482297%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
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