Glucocerebrosidase mutations in Chinese subjects from Taiwan with sporadic Parkinson disease
- 25 April 2007
- journal article
- research article
- Published by Elsevier in Molecular Genetics and Metabolism
- Vol. 91 (2) , 195-200
- https://doi.org/10.1016/j.ymgme.2007.03.004
Abstract
No abstract availableKeywords
This publication has 33 references indexed in Scilit:
- A common LRRK2 mutation in idiopathic Parkinson's diseaseThe Lancet, 2005
- Parkinsonism among Gaucher disease carriersJournal of Medical Genetics, 2004
- Mutations in the Glucocerebrosidase Gene and Parkinson's Disease in Ashkenazi JewsNew England Journal of Medicine, 2004
- Cloning of the Gene Containing Mutations that Cause PARK8-Linked Parkinson's DiseaseNeuron, 2004
- Mutations in LRRK2 Cause Autosomal-Dominant Parkinsonism with Pleomorphic PathologyNeuron, 2004
- Pilot association study of the β‐glucocerebrosidase N370S allele and Parkinson's disease in subjects of Jewish ethnicityMovement Disorders, 2004
- Mutations in the DJ-1 Gene Associated with Autosomal Recessive Early-Onset ParkinsonismScience, 2003
- Genetics of parkinsonismMovement Disorders, 2002
- The α-Synuclein Gene and Parkinson Disease in a Chinese PopulationArchives of Neurology, 2000
- Mutations in the parkin gene cause autosomal recessive juvenile parkinsonismNature, 1998