The dardarin G2019S mutation is a common cause of Parkinson's disease but not other neurodegenerative diseases-Reference-Cited by-同舟云学术

The dardarin G2019S mutation is a common cause of Parkinson's disease but not other neurodegenerative diseases

Published:2005-12 Issue:3 Volume:389 Page:137-139
ISSN:0304-3940
Container-title:Neuroscience Letters
language:en
Short-container-title:Neuroscience Letters

Author:

Hernandez Dena,Paisan Ruiz Coro,Crawley Anthony,Malkani Roneil,Werner John,Gwinn-Hardy Katrina,Dickson Dennis,Wavrant DeVrieze Fabienne,Hardy John,Singleton Andrew

Publisher

Elsevier BV

Subject

General Neuroscience

Reference19 articles.

1. Clinical features of LRRK2-associated Parkinson's disease in central Norway;Aasly;Ann. Neurol.,2005

2. J.M. Bras, R.J. Guerreiro, M.H. Ribeiro, C. Januario, A. Morgadinho, C.R. Oliveira, L. Cunha, J. Hardy, A. Singleton, Mutations in LRRK2 are a common cause of Parkinson's disease in a Portuguese cohort, Mov. Disord., in press.

3. A population perspective on diagnostic criteria for Parkinson's disease;de Rijk;Neurology,1997

4. A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease;Di Fonzo;Lancet,2005

5. An LRRK2 mutation as a cause for the parkinsonism in the original PARK8 family;Funayama;Ann. Neurol.,2005

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