A common LRRK2 mutation in idiopathic Parkinson's disease-Reference-Cited by-同舟云学术

A common LRRK2 mutation in idiopathic Parkinson's disease

Published:2005-01 Issue:9457 Volume:365 Page:415-416
ISSN:0140-6736
Container-title:The Lancet
language:en
Short-container-title:The Lancet

Author:

Gilks William P,Abou-Sleiman Patrick M,Gandhi Sonia,Jain Shushant,Singleton Andrew,Lees Andrew J,Shaw Karen,Bhatia Kailash P,Bonifati Vincenzo,Quinn Niall P,Lynch John,Healy Daniel G,Holton Janice L,Revesz Tamas,Wood Nicholas W

Publisher

Elsevier BV

Subject

General Medicine

Reference5 articles.

1. Genetic clues to the pathogenesis of Parkinson's;Vila;Nat Med,2004

2. Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease;Paisan-Ruiz;Neuron,2004

3. Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology;Zimprich;Neuron,2004

4. Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases;Hughes;J Neurol Neurosurg Psychiatry,1992

5. PINK, PANK, or PARK? A clinicians' guide to familial parkinsonism;Healy;Lancet Neurol,2004

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