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English
Exonic deletion mutations of the Parkin gene among sporadic patients with Parkinson's disease
scientific article published on 01 July 2000
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
10817951
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10817951%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 November 2019
title
Exonic deletion mutations of the Parkin gene among sporadic patients with Parkinson's disease
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
10817951
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10817951%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 November 2019
main subject
Parkinson's disease
1 reference
based on heuristic
inferred from title
author name string
Kobayashi T
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
10817951
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10817951%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 November 2019
Wang M
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
10817951
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10817951%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 November 2019
Hattori N
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
10817951
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10817951%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 November 2019
Matsumine H
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed ID
10817951
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10817951%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 November 2019
Kondo T
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed ID
10817951
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10817951%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 November 2019
Mizuno Y
series ordinal
6
1 reference
stated in
Europe PubMed Central
PubMed ID
10817951
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10817951%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 November 2019
publication date
1 July 2000
1 reference
stated in
Europe PubMed Central
PubMed ID
10817951
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10817951%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 November 2019
number of pages
3
1 reference
based on heuristic
inferred from page(s)
published in
Parkinsonism and Related Disorders
1 reference
stated in
Europe PubMed Central
PubMed ID
10817951
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10817951%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 November 2019
volume
6
1 reference
stated in
Europe PubMed Central
PubMed ID
10817951
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10817951%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 November 2019
issue
3
1 reference
stated in
Europe PubMed Central
PubMed ID
10817951
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10817951%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 November 2019
page(s)
129-131
1 reference
stated in
Europe PubMed Central
PubMed ID
10817951
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10817951%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 November 2019
cites work
Clinical, pathologic and genetic studies on autosomal recessive early-onset parkinsonism with diurnal fluctuation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1353-8020%2800%2900006-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1353-8020%2800%2900006-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular genetic analysis of a novelParkin gene in Japanese families with autosomal recessive juvenile parkinsonism: Evidence for variable homozygous deletions in theParkin gene in affected individuals
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1353-8020%2800%2900006-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Parkinsonism: onset, progression, and mortality
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1353-8020%2800%2900006-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S1353-8020(00)00006-7
1 reference
stated in
Europe PubMed Central
PubMed ID
10817951
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10817951%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 November 2019
PubMed ID
10817951
1 reference
stated in
Europe PubMed Central
PubMed ID
10817951
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10817951%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 November 2019
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