PINK1 mutations in sporadic early-onset Parkinson's disease-Reference-Cited by-同舟云学术

PINK1 mutations in sporadic early-onset Parkinson's disease

Published:2006-02-15 Issue:6 Volume:21 Page:789-793
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov. Disord.

Author:

Tan Eng-King,Yew Kenneth,Chua Eva,Puvan K.,Shen Hui,Lee Esther,Puong Kim-Yoong,Zhao Yi,Pavanni Ratnagopal,Wong Meng-Cheong,Jamora Dominic,de Silva Deidre,Moe Kyaw-Thu,Woon Fung-Peng,Yuen Yih,Tan Louis

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference19 articles.

1. New aspects of genetic contributions to Parkinson's disease;Hofer;J Mol Neurosci,2004

2. Hereditary early-onset Parkinson's disease caused by mutations in PINK1;Valente;Science,2004

3. Variability and validity of polymorphism association studies in Parkinson's disease;Tan;Neurology,2000

4. Analysis of the PINK1 gene in a large cohort of cases with Parkinson disease;Rogaeva;Arch Neurol,2004

5. PINK1 (PARK6) associated Parkinson disease in Ireland;Healy;Neurology,2004

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