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

KRÜGER, Rejko; Kuhn, W.; Muller, T.; Woitalla, D.; Graeber, M.; Kosel, S.; Przuntek, H.; Epplen, J. T.; Schols, L.; Riess, O.

doi:10.1038/ng0298-106

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Article (Scientific journals)

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

KRÜGER, Rejko; Kuhn, W.; Muller, T. et al.

1998 • In Nature genetics, 18 (2), p. 106-8

Peer reviewed

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https://hdl.handle.net/10993/17109

DOI
10.1038/ng0298-106

PubMed
9462735

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Keywords :

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 center :

- Luxembourg Centre for Systems Biomedicine (LCSB): Clinical & Experimental Neuroscience (Krüger Group)

Disciplines :

Genetics & genetic processes

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.

Language :

English

Title :

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

Publication date :

1998

Journal title :

Nature genetics

ISSN :

1061-4036

Volume :

Issue :

Pages :

106-8

Peer reviewed :

Peer reviewed

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since 27 June 2014

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