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Parkin-related disease clinically diagnosed as a pallido-pyramidal syndrome.

作者信息

Wickremaratchi Mindhu M, Majounie Elisa, Morris Huw R, Williams Nigel M, Lewis Helen, Gill Steven S, Khan Sadaquate, Heywood Peter, Hardy John, Wiles Charles M, Singleton Andrew B, Quinn Niall P

出版信息

Mov Disord. 2009 Jan 15;24(1):138-40. doi: 10.1002/mds.22181.

Abstract
摘要

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本文引用的文献

1
Genomewide SNP assay reveals mutations underlying Parkinson disease.
Hum Mutat. 2008 Feb;29(2):315-22. doi: 10.1002/humu.20626.
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Genetics of Parkinson's disease and parkinsonism.
Ann Neurol. 2006 Oct;60(4):389-98. doi: 10.1002/ana.21022.
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Deletion of the parkin and PACRG gene promoter in early-onset parkinsonism.
Hum Mutat. 2007 Jan;28(1):27-32. doi: 10.1002/humu.20436.
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Lewy body Parkinson's disease in a large pedigree with 77 Parkin mutation carriers.
Ann Neurol. 2005 Sep;58(3):411-22. doi: 10.1002/ana.20587.
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Searching for a relationship between manganese and welding and Parkinson's disease.
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Distribution, type, and origin of Parkin mutations: review and case studies.
Mov Disord. 2004 Oct;19(10):1146-57. doi: 10.1002/mds.20234.
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Parkin-positive autosomal recessive juvenile Parkinsonism with alpha-synuclein-positive inclusions.
Neurology. 2004 Aug 24;63(4):678-82. doi: 10.1212/01.wnl.0000134657.25904.0b.
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parkin mutation analysis in clinic patients with early-onset Parkinson [corrected] disease.
Am J Med Genet A. 2004 Aug 15;129A(1):44-50. doi: 10.1002/ajmg.a.30157.

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