Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease.

Reference : Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease.


	Document type :	Scientific journals : Article
	Discipline(s) :	Life sciences : Genetics & genetic processes
	To cite this reference:	http://hdl.handle.net/10993/17109

Title :	Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease.
Language :	English
Author, co-author :	Krüger, Rejko [University of Luxembourg > Faculty of Science, Technology and Communication (FSTC) > Life Science Research Unit]
	Kuhn, W. [> >]
	Muller, T. [> >]
	Woitalla, D. [> >]
	Graeber, M. [> >]
	Kosel, S. [> >]
	Przuntek, H. [> >]
	Epplen, J. T. [> >]
	Schols, L. [> >]
	Riess, O. [> >]
Publication date :	1998
Journal title :	Nature genetics
Volume :	18
Issue/season :	2
Pages :	106-8
Peer reviewed :	Yes (verified by ORBi^lu)
ISSN :	1061-4036
Country :	UNITED STATES
Keywords :	[en] Alanine ; Amino Acid Sequence ; Base Sequence ; Female ; Humans ; Male ; Nerve Tissue Proteins/chemistry/genetics ; Parkinson Disease/genetics ; Pedigree ; Point Mutation ; Polymorphism, Single-Stranded Conformational ; Proline ; Synucleins ; alpha-Synuclein
Research centres :	Luxembourg Centre for Systems Biomedicine (LCSB): Clinical & Experimental Neuroscience (Krüger Group)
Permalink :	http://hdl.handle.net/10993/17109
DOI :	10.1038/ng0298-106

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