(Q34460129)

2 August 2017

A susceptibility locus for Parkinson's disease maps to chromosome 2p13. (English)

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2 August 2017

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5

Calne DB

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2 August 2017

3

Wszolek ZK

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2 August 2017

Gasser T

1

1 reference

2 August 2017

Müller-Myhsok B

2

1 reference

2 August 2017

Oehlmann R

4

1 reference

2 August 2017

Bonifati V

6

1 reference

2 August 2017

Bereznai B

7

1 reference

2 August 2017

Fabrizio E

8

1 reference

2 August 2017

Vieregge P

9

1 reference

2 August 2017

Horstmann RD

10

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2 August 2017

language of work or name

English

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publication date

1 March 1998

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2 August 2017

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2 August 2017

18

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2 August 2017

262-265

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2 August 2017

3

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https://scigraph.springernature.com/pub.10.1038/ng0398-262

2 August 2017

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cites work

Mapping of a gene for Parkinson's disease to chromosome 4q21-q23

1 reference

https://api.crossref.org/works/10.1038%2FNG0398-262

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0398-262

Familial parkinsonism: Our experience and review

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0398-262

A comprehensive genetic map of the human genome based on 5,264 microsatellites

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0398-262

Human neutral amino acid transporter ASCT1: structure of the gene (SLC1A4) and localization to chromosome 2p13-p15.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0398-262

Trophic actions of transforming growth factor alpha on mesencephalic dopaminergic neurons developing in culture

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0398-262

Genetic factors in the etiology of idiopathic Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0398-262

7 January 2021

Genes and parkinsonism.

1 reference

https://api.crossref.org/works/10.1038%2FNG0398-262

7 January 2021

A large kindred with autosomal dominant Parkinson's disease

1 reference

https://api.crossref.org/works/10.1038%2FNG0398-262

7 January 2021

Western Nebraska family (family D) with autosomal dominant parkinsonism

1 reference

https://api.crossref.org/works/10.1038%2FNG0398-262

7 January 2021

Clinical genetic analysis of Parkinson's disease in the Contursi kindred

1 reference

https://api.crossref.org/works/10.1038%2FNG0398-262

7 January 2021

German-Canadian family (family A) with parkinsonism, amyotrophy, and dementia - Longitudinal observations

1 reference

https://api.crossref.org/works/10.1038%2FNG0398-262

7 January 2021

Familial parkinsonism, dementia, and Lewy body disease: study of family G.

1 reference

https://api.crossref.org/works/10.1038%2FNG0398-262

7 January 2021

The relevance of the Lewy body to the pathogenesis of idiopathic Parkinson's disease

1 reference

https://api.crossref.org/works/10.1038%2FNG0398-262

7 January 2021

Genetic dissection of complex traits

1 reference

https://api.crossref.org/works/10.1038%2FNG0398-262

7 January 2021

Genetic linkage studies in autosomal dominant parkinsonism: evaluation of seven candidate genes

1 reference

https://api.crossref.org/works/10.1038%2FNG0398-262

7 January 2021

Sets of short tandem repeat polymorphisms for efficient linkage screening of the human genome

1 reference

https://api.crossref.org/works/10.1038%2FNG0398-262

7 January 2021

Avoiding recomputation in linkage analysis.

1 reference

https://api.crossref.org/works/10.1038%2FNG0398-262

7 January 2021

The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance

1 reference

https://api.crossref.org/works/10.1038%2FNG0398-262

7 January 2021

Identifiers

DOI

10.1038/NG0398-262

1 reference

2 August 2017

1 reference