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PMID: 16788020 Published · ppublish English Letter Research Support, Non-U.S. Gov't

The LRRK2 gene in Parkinson's disease: mutation screening in patients from Germany.

Journal of neurology, neurosurgery, and psychiatry ·Vol. 77 ·No. 7 ·2006-07-00 ·Pages 891-2

Schlitter AM, Woitalla D, Mueller T, Epplen JT, Dekomien G

Abstract

暂无摘要

MeSH Terms
Adult Age of Onset Aged, 80 and over Cohort Studies DNA Mutational Analysis Female Genetic Predisposition to Disease Genetic Testing Germany Humans Leucine-Rich Repeat Serine-Threonine Protein Kinase-2 Male Middle Aged Parkinson Disease/genetics Protein Serine-Threonine Kinases/genetics
Chemicals
LRRK2 protein, human Leucine-Rich Repeat Serine-Threonine Protein Kinase-2 Protein Serine-Threonine Kinases
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Schlitter A M
Woitalla D
Mueller T
Epplen J T
Dekomien G
References (5)
5 references, click to expand
  1. Protein kinases linked to the pathogenesis of Parkinson's disease.
    Neuron. 2004 Nov 18;44(4):575-7 PMID: 15541303
  2. Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease.
    Neuron. 2004 Nov 18;44(4):595-600 PMID: 15541308
  3. Escaping Parkinson's disease: a neurologically healthy octogenarian with the LRRK2 G2019S mutation.
    Mov Disord. 2005 Aug;20(8):1077-8 PMID: 16001413
  4. Altered alpha-synuclein homeostasis causing Parkinson's disease: the potential roles of dardarin.
    Trends Neurosci. 2005 Aug;28(8):416-21 PMID: 15955578
  5. A common LRRK2 mutation in idiopathic Parkinson's disease.
    Lancet. 2005 Jan 29-Feb 4;365(9457):415-6 PMID: 15680457
Article Info
Journal
Journal of neurology, neurosurgery, and psychiatry
Abbr.
J Neurol Neurosurg Psychiatry
ISSN
1468-330X
DOI
10.1136/jnnp.2005.083022
Published
2006-07-00
Pages
891-2
Language
English
Region
England
NLM ID
2985191R
PMCID
PMC2117481
Subset
IM
External Links
PubMed source DOI: 10.1136/jnnp.2005.083022 PMC Full Text View journal details
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