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English
Screening for mutations in synaptotagmin XI in Parkinson's disease.
scientific article
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
15354386
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15354386%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
title
Screening for mutations in synaptotagmin XI in Parkinson's disease
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
15354386
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15354386%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
main subject
Parkinson's disease
1 reference
based on heuristic
inferred from title
author
Daniela Berg
1 reference
stated in
ORCID Public Data File 2021
author name string
A S Glass
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
15354386
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15354386%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
D P Huynh
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
15354386
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15354386%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
Th Franck
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
15354386
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15354386%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
D Woitalla
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed ID
15354386
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15354386%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
Th Müller
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed ID
15354386
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15354386%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
S M Pulst
series ordinal
6
1 reference
stated in
Europe PubMed Central
PubMed ID
15354386
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15354386%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
D Berg
series ordinal
7
1 reference
stated in
Europe PubMed Central
PubMed ID
15354386
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15354386%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
R Krüger
series ordinal
8
1 reference
stated in
Europe PubMed Central
PubMed ID
15354386
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15354386%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
O Riess
series ordinal
9
1 reference
stated in
Europe PubMed Central
PubMed ID
15354386
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15354386%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
publication date
1 January 2004
1 reference
stated in
Europe PubMed Central
PubMed ID
15354386
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15354386%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
published in
Journal of neural transmission. Supplementum
1 reference
stated in
Europe PubMed Central
PubMed ID
15354386
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15354386%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
page(s)
21-28
1 reference
stated in
Europe PubMed Central
PubMed ID
15354386
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15354386%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
issue
68
1 reference
stated in
Europe PubMed Central
PubMed ID
15354386
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15354386%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
cites work
Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism
1 reference
stated in
COCI
retrieved
4 November 2023
reference URL
https://opencitations.net/index/coci/api/v1/citations/10.1038/33416
Identifiers
DOI
10.1007/978-3-7091-0579-5_3
1 reference
stated in
Europe PubMed Central
PubMed ID
15354386
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15354386%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
PubMed ID
15354386
1 reference
stated in
Europe PubMed Central
PubMed ID
15354386
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15354386%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
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