(Q73532938)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11215568%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

title

Prevalence of homozygous deletions of the parkin gene in a cohort of patients with sporadic and familial Parkinson's disease (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11215568%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

1 reference

1 reference

H Ujike

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11215568%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

M Yamamoto

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11215568%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

A Kanzaki

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11215568%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

K Okumura

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11215568%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

M Takaki

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11215568%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

S Kuroda

6

1 reference

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4 November 2019

publication date

1 January 2001

1 reference

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4 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11215568%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

volume

16

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11215568%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

issue

1

1 reference

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4 November 2019

page(s)

111-113

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11215568%20AND%20SRC:MED&resulttype=core&format=json

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

4 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1002%2F1531-8257%28200101%2916%3A1%3C111%3A%3AAID-MDS1023%3E3.0.CO%3B2-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8257%28200101%2916%3A1%3C111%3A%3AAID-MDS1023%3E3.0.CO%3B2-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8257%28200101%2916%3A1%3C111%3A%3AAID-MDS1023%3E3.0.CO%3B2-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8257%28200101%2916%3A1%3C111%3A%3AAID-MDS1023%3E3.0.CO%3B2-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8257%28200101%2916%3A1%3C111%3A%3AAID-MDS1023%3E3.0.CO%3B2-6

Paralysis agitans of early onset with marked diurnal fluctuation of symptoms

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8257%28200101%2916%3A1%3C111%3A%3AAID-MDS1023%3E3.0.CO%3B2-6

Mutation in the alpha-synuclein gene identified in families with Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8257%28200101%2916%3A1%3C111%3A%3AAID-MDS1023%3E3.0.CO%3B2-6

The ubiquitin pathway in Parkinson's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8257%28200101%2916%3A1%3C111%3A%3AAID-MDS1023%3E3.0.CO%3B2-6

Analysis of the parkin deletion in sporadic and familial Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8257%28200101%2916%3A1%3C111%3A%3AAID-MDS1023%3E3.0.CO%3B2-6

10.1002/1531-8257(200101)16:1<111::AID-MDS1023>3.0.CO;2-6

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11215568%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

1 reference