Parkinson's disease and LRRK2: frequency of a common mutation in U.S. movement disorder clinics (Q46775406)

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English	Parkinson's disease and LRRK2: frequency of a common mutation in U.S. movement disorder clinics	scientific article

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scholarly article

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Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/16250030

Parkinson's disease and LRRK2: frequency of a common mutation in U.S. movement disorder clinics (English)

1 reference

Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/16250030

Parkinson's disease

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based on heuristic

inferred from title

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Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/16250030

Cyrus P Zabetian

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Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/16250030

4

object named as

John G Nutt

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Europe PubMed Central

PubMed publication ID

25 December 2017

Stewart A Factor

3

object named as

Stewart A Factor

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Europe PubMed Central

PubMed publication ID

25 December 2017

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object named as

Ali Samii

1 reference

Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/16250030

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object named as

Haydeh Payami

1 reference

Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/16250030

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object named as

Alida Griffith

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Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/16250030

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object named as

Tom D Bird

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Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/16250030

Patricia Ann Kramer

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object named as

Patricia Kramer

1 reference

Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/16250030

author name string

Donald S Higgins

9

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Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/16250030

language of work or name

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publication date

1 April 2006

1 reference

Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/16250030

Movement Disorders

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Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/16250030

21

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Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/16250030

4

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Europe PubMed Central

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25 December 2017

http://europepmc.org/abstract/MED/16250030

519-523

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Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/16250030

A new locus for Parkinson's disease (PARK8) maps to chromosome 12p11.2-q13.1.

1 reference

https://api.crossref.org/works/10.1002%2FMDS.20751

21 January 2018

Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease

1 reference

https://api.crossref.org/works/10.1002%2FMDS.20751

21 January 2018

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

1 reference

https://api.crossref.org/works/10.1002%2FMDS.20751

21 January 2018

Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations

1 reference

https://api.crossref.org/works/10.1002%2FMDS.20751

21 January 2018

Clinical features of LRRK2-associated Parkinson's disease in central Norway

1 reference

https://api.crossref.org/works/10.1002%2FMDS.20751

21 January 2018

Familial aggregation of Parkinson disease: a comparative study of early-onset and late-onset disease

1 reference

https://api.crossref.org/works/10.1002%2FMDS.20751

21 January 2018

Escaping Parkinson's disease: a neurologically healthy octogenarian with the LRRK2 G2019S mutation

1 reference

https://api.crossref.org/works/10.1002%2FMDS.20751

21 January 2018

Distribution, type, and origin of Parkin mutations: review and case studies

1 reference

https://api.crossref.org/works/10.1002%2FMDS.20751

21 January 2018

The current status of Alzheimer's disease genetics: what do we tell the patients?

1 reference

https://api.crossref.org/works/10.1002%2FMDS.20751

21 January 2018

Effects of age, sex, and ethnicity on the association between apolipoprotein E genotype and Alzheimer disease. A meta-analysis. APOE and Alzheimer Disease Meta Analysis Consortium

1 reference

https://api.crossref.org/works/10.1002%2FMDS.20751

21 January 2018

Identifiers

10.1002/MDS.20751

1 reference

Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/16250030

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/16250030

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