(Q77087748)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11684352%20AND%20SRC:MED&resulttype=core&format=json

2 December 2019

title

Early-onset Parkinson's disease associated with a new parkin mutation in a Spanish family (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11684352%20AND%20SRC:MED&resulttype=core&format=json

2 December 2019

1 reference

V Alvarez

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11684352%20AND%20SRC:MED&resulttype=core&format=json

2 December 2019

L M Guisasola

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11684352%20AND%20SRC:MED&resulttype=core&format=json

2 December 2019

V G Moreira

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11684352%20AND%20SRC:MED&resulttype=core&format=json

2 December 2019

C H Lahoz

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11684352%20AND%20SRC:MED&resulttype=core&format=json

2 December 2019

E Coto

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11684352%20AND%20SRC:MED&resulttype=core&format=json

2 December 2019

publication date

1 November 2001

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11684352%20AND%20SRC:MED&resulttype=core&format=json

2 December 2019

number of pages

3

1 reference

inferred from page(s)

published in

Neuroscience Letters

1 reference

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2 December 2019

volume

313

1 reference

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2 December 2019

issue

1-2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11684352%20AND%20SRC:MED&resulttype=core&format=json

2 December 2019

page(s)

108-110

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11684352%20AND%20SRC:MED&resulttype=core&format=json

A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease

2 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2801%2902235-2

7 January 2021

Point mutations (Thr240Arg and Gln311Stop) [correction of Thr240Arg and Ala311Stop] in the Parkin gene.

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2801%2902235-2

7 January 2021

Parkin is associated with actin filaments in neuronal and nonneural cells

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2801%2902235-2

7 January 2021

Does failure of parkin-mediated ubiquitination cause juvenile parkinsonism?

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2801%2902235-2

7 January 2021

Putting the parkin into Parkinson's

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2801%2902235-2

7 January 2021

Progress in the clinical and molecular genetics of familial parkinsonism

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2801%2902235-2

7 January 2021

Deletions in the Parkin gene and genetic heterogeneity in a Greek family with early onset Parkinson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2801%2902235-2

7 January 2021

Homozygous deletions in parkin gene in European and North African families with autosomal recessive juvenile parkinsonism. The European Consortium on Genetic Susceptibility in Parkinson's Disease and the French Parkinson's Disease Genetics Study Gro

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2801%2902235-2

7 January 2021

Association between early-onset Parkinson's disease and mutations in the parkin gene

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2801%2902235-2

7 January 2021

Novel mutations, pseudo-dominant inheritance, and possible familial affects in patients with autosomal recessive juvenile parkinsonism

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2801%2902235-2

7 January 2021

A new mutation in the parkin gene in a patient with atypical autosomal recessive juvenile parkinsonism

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2801%2902235-2

7 January 2021

Origin of the mutations in the parkin gene in Europe: exon rearrangements are independent recurrent events, whereas point mutations may result from Founder effects

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2801%2902235-2

7 January 2021

Familial Parkinson disease gene product, parkin, is a ubiquitin-protein ligase

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2801%2902235-2

7 January 2021

New mutation (R42P) of the parkin gene in the ubiquitinlike domain associated with parkinsonism

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2801%2902235-2

7 January 2021

Clinical and pathologic abnormalities in a family with parkinsonism and parkin gene mutations.

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2801%2902235-2

7 January 2021

Parkin functions as an E2-dependent ubiquitin- protein ligase and promotes the degradation of the synaptic vesicle-associated protein, CDCrel-1

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2801%2902235-2

7 January 2021

10.1016/S0304-3940(01)02235-2

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11684352%20AND%20SRC:MED&resulttype=core&format=json

2 December 2019

1 reference