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English
A novel form of autosomal recessive hereditary spastic paraplegia caused by a new SPG7 mutation.
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
17646629
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17646629%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 January 2020
title
A novel form of autosomal recessive hereditary spastic paraplegia caused by a new SPG7 mutation
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
17646629
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17646629%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 January 2020
main subject
hereditary spastic paraplegia
1 reference
based on heuristic
inferred from title
author
Joerg T. Epplen
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed ID
17646629
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17646629%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 January 2020
author name string
Warnecke T
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
17646629
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17646629%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 January 2020
Duning T
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
17646629
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17646629%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 January 2020
Schwan A
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
17646629
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17646629%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 January 2020
Lohmann H
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed ID
17646629
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17646629%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 January 2020
Young P
series ordinal
6
1 reference
stated in
Europe PubMed Central
PubMed ID
17646629
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17646629%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 January 2020
language of work or name
English
0 references
publication date
1 July 2007
1 reference
stated in
Europe PubMed Central
PubMed ID
17646629
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17646629%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 January 2020
published in
Neurology
1 reference
stated in
Europe PubMed Central
PubMed ID
17646629
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17646629%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 January 2020
volume
69
1 reference
stated in
Europe PubMed Central
PubMed ID
17646629
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17646629%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 January 2020
issue
4
1 reference
stated in
Europe PubMed Central
PubMed ID
17646629
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17646629%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 January 2020
page(s)
368-375
1 reference
stated in
Europe PubMed Central
PubMed ID
17646629
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17646629%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 January 2020
Identifiers
DOI
10.1212/01.WNL.0000266667.91074.FE
1 reference
stated in
Europe PubMed Central
PubMed ID
17646629
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17646629%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 January 2020
PubMed ID
17646629
1 reference
stated in
Europe PubMed Central
PubMed ID
17646629
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17646629%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 January 2020
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