G2019S dardarin substitution is a common cause of Parkinson's disease in a Portuguese cohort-Reference-Cited by-同舟云学术

G2019S dardarin substitution is a common cause of Parkinson's disease in a Portuguese cohort

Published:2005-09-07 Issue:12 Volume:20 Page:1653-1655
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov. Disord.

Author:

Bras Jose Miguel¹²³,Guerreiro Rita Joao¹²³,Ribeiro Maria Helena¹²,Januario Cristina¹,Morgadinho Ana¹,Oliveira Catarina Resende¹²,Cunha Luis¹,Hardy John³,Singleton Andrew³

Affiliation:

1. Neurology Service, Coimbra University Hospital, Coimbra, Portugal

2. Institute of Biochemistry, Faculty of Medicine, Center for Neurosciences and Cell Biology, University of Coimbra, Coimbra, Portugal

3. Laboratory of Neurogenetics, National Institutes on Aging, National Institutes of Health, Bethesda, Maryland, USA

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mds.20682

Reference14 articles.

1. Mutation in the α-Synuclein Gene Identified in Families with Parkinson's Disease

2. Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

3. Mutations in the DJ-1 Gene Associated with Autosomal Recessive Early-Onset Parkinsonism

4. Hereditary Early-Onset Parkinson's Disease Caused by Mutations in PINK1

5. Genetic testing in Parkinson's disease

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