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English
The CNTN4 c.4256C>T mutation is rare in Japanese with inherited spinocerebellar ataxia.
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17915252
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17915252%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
title
The CNTN4 c.4256C>T mutation is rare in Japanese with inherited spinocerebellar ataxia
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17915252
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17915252%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
author
Hirofumi Maruyama
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17915252
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17915252%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
Hiroyuki Morino
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17915252
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17915252%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
Hideshi Kawakami
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17915252
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17915252%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
author name string
Eiji Tanaka
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17915252
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17915252%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
Eiko Nakajima
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17915252
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17915252%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
publication date
2 October 2007
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17915252
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17915252%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
published in
Journal of the Neurological Sciences
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17915252
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17915252%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
volume
266
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17915252
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17915252%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
issue
1-2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17915252
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17915252%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
page(s)
180-181
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17915252
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17915252%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
Identifiers
DOI
10.1016/J.JNS.2007.09.004
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17915252
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17915252%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
PubMed publication ID
17915252
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17915252
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17915252%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
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