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Cockayne syndrome group B (Csb) and group a (Csa) deficiencies predispose to hearing loss and cochlear hair cell degeneration in mice.
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Europe PubMed Central
PMC publication ID
4355199
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25762674%20AND%20SRC:MED&resulttype=core&format=json
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2 March 2020
title
Cockayne syndrome group B (Csb) and group a (Csa) deficiencies predispose to hearing loss and cochlear hair cell degeneration in mice
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
4355199
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25762674%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 March 2020
main subject
hearing loss
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Cockayne syndrome
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author
Andries Paul Nagtegaal
series ordinal
1
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Europe PubMed Central
PMC publication ID
4355199
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25762674%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 March 2020
Robert N Rainey
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2
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4355199
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25762674%20AND%20SRC:MED&resulttype=core&format=json
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2 March 2020
Ingrid van der Pluijm
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3
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Europe PubMed Central
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4355199
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2 March 2020
Gijsbertus van der Horst
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5
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4355199
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25762674%20AND%20SRC:MED&resulttype=core&format=json
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2 March 2020
author name string
Renata M C Brandt
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4
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Europe PubMed Central
PMC publication ID
4355199
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25762674%20AND%20SRC:MED&resulttype=core&format=json
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2 March 2020
J Gerard G Borst
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6
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4355199
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2 March 2020
Neil Segil
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7
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4355199
reference URL
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retrieved
2 March 2020
language of work or name
English
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publication date
1 March 2015
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Europe PubMed Central
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4355199
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retrieved
2 March 2020
published in
Journal of Neuroscience
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PMC publication ID
4355199
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25762674%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 March 2020
volume
35
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4355199
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25762674%20AND%20SRC:MED&resulttype=core&format=json
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2 March 2020
issue
10
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Europe PubMed Central
PMC publication ID
4355199
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25762674%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 March 2020
page(s)
4280-4286
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Europe PubMed Central
PMC publication ID
4355199
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25762674%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 March 2020
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Europe PubMed Central
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11 June 2022
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Cockayne syndrome in adults: review with clinical and pathologic study of a new case
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Association of cadherin 23 with polygenic inheritance and genetic modification of sensorineural hearing loss
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Molecular analysis of mutations in the CSB (ERCC6) gene in patients with Cockayne syndrome
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Defective transcription-coupled repair in Cockayne syndrome B mice is associated with skin cancer predisposition
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UVB radiation-induced cancer predisposition in Cockayne syndrome group A (Csa) mutant mice.
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Cockayne syndrome--an audiologic and temporal bone analysis
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Identifiers
DOI
10.1523/JNEUROSCI.5063-14.2015
1 reference
stated in
Europe PubMed Central
PMC publication ID
4355199
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25762674%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 March 2020
PMC publication ID
4355199
1 reference
stated in
Europe PubMed Central
PMC publication ID
4355199
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25762674%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 March 2020
PubMed publication ID
25762674
1 reference
stated in
Europe PubMed Central
PMC publication ID
4355199
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25762674%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 March 2020
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