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English
An LRRK2 mutation as a cause for the parkinsonism in the original PARK8 family.
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
15880653
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15880653%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 January 2020
title
An LRRK2 mutation as a cause for the parkinsonism in the original PARK8 family
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
15880653
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15880653%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 January 2020
main subject
Parkinson's disease
2 references
based on heuristic
inferred from title
based on heuristic
inferred from title
parkinsonian syndrome
1 reference
based on heuristic
inferred from title
author
Manabu Funayama
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
15880653
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15880653%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 January 2020
author name string
Kazuko Hasegawa
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
15880653
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15880653%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 January 2020
Etsuro Ohta
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
15880653
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15880653%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 January 2020
Noriko Kawashima
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed ID
15880653
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15880653%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 January 2020
Masaru Komiyama
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed ID
15880653
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15880653%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 January 2020
Hisayuki Kowa
series ordinal
6
1 reference
stated in
Europe PubMed Central
PubMed ID
15880653
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15880653%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 January 2020
Shoji Tsuji
series ordinal
7
1 reference
stated in
Europe PubMed Central
PubMed ID
15880653
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15880653%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 January 2020
Fumiya Obata
series ordinal
8
1 reference
stated in
Europe PubMed Central
PubMed ID
15880653
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15880653%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 January 2020
publication date
1 June 2005
1 reference
stated in
Europe PubMed Central
PubMed ID
15880653
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15880653%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 January 2020
published in
Annals of Neurology
1 reference
stated in
Europe PubMed Central
PubMed ID
15880653
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15880653%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 January 2020
volume
57
1 reference
stated in
Europe PubMed Central
PubMed ID
15880653
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15880653%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 January 2020
issue
6
1 reference
stated in
Europe PubMed Central
PubMed ID
15880653
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15880653%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 January 2020
page(s)
918-921
1 reference
stated in
Europe PubMed Central
PubMed ID
15880653
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15880653%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 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
10.1002/ANA.20484
1 reference
stated in
Europe PubMed Central
PubMed ID
15880653
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15880653%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 January 2020
PubMed ID
15880653
1 reference
stated in
Europe PubMed Central
PubMed ID
15880653
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15880653%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 January 2020
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