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PMID: 16251215 Published · ppublish English Journal Article

Type and frequency of mutations in the LRRK2 gene in familial and sporadic Parkinson's disease*.

Brain : a journal of neurology ·Vol. 128 ·No. Pt 12 ·2005-12-00 ·Pages 3000-11

Berg D, Schweitzer KJ, Leitner P, Zimprich A, Lichtner P, Belcredi P, Brüssel T, Schulte C, Maass S, Nägele T, Wszolek ZK, Gasser T

Abstract

暂无摘要

MeSH Terms
Adult Brain/pathology Case-Control Studies DNA Mutational Analysis DNA Primers Echoencephalography Exons Female Genes, Dominant Haplotypes Humans Leucine-Rich Repeat Serine-Threonine Protein Kinase-2 Magnetic Resonance Imaging Male Middle Aged Mutation, Missense/genetics Neuropsychological Tests Parkinson Disease/diagnostic imaging,genetics,pathology Pedigree Penetrance Protein Serine-Threonine Kinases/genetics Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
Chemicals
DNA Primers LRRK2 protein, human Leucine-Rich Repeat Serine-Threonine Protein Kinase-2 Protein Serine-Threonine Kinases
Authors & Affiliations
12 authors, click to expand affiliations / ORCID
Berg Daniela
Schweitzer Katherine J
Leitner Petra
Zimprich Alexander
Lichtner Peter
Belcredi Petra
Brüssel Theresa
Schulte Claudia
Maass Sylvia
Nägele Thomas
Wszolek Zbigniew K
Gasser Thomas
Article Info
Journal
Brain : a journal of neurology
Abbr.
Brain
ISSN
1460-2156
Published
2005-12-00
Pages
3000-11
Language
English
Region
England
NLM ID
0372537
Subset
IM
Corrections
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