Unraveling the role of defective genes in Parkinson's disease

Research output: Contribution to journalArticle

Abstract

Parkinson's disease (PD) is a common neurodegenerative disease characterized by the loss of dopaminergic neurons leading to bradykinesia, rest tremor and rigidity. Although the majority of PD is sporadic, rare genetic causes of PD are providing tremendous insight into the pathogenesis of PD. Here I shortly review the major genes implicated in autosomal dominant and autosomal recessive PD. Understanding how mutations in these PD associated genes holds particular promise for development of new therapies to treat PD.

Original languageEnglish (US)
JournalParkinsonism and Related Disorders
Volume13
Issue numberSUPPL. 3
DOIs
StatePublished - 2007

Fingerprint

Parkinson Disease
Genes
Hypokinesia
Dopaminergic Neurons
Tremor
Neurodegenerative Diseases
Mutation

Keywords

  • a-synuclein
  • DJ-1
  • LRRK2
  • parkin
  • PINK1

ASJC Scopus subject areas

  • Aging
  • Clinical Neurology
  • Neurology

Cite this

Unraveling the role of defective genes in Parkinson's disease. / Dawson, Ted M.

In: Parkinsonism and Related Disorders, Vol. 13, No. SUPPL. 3, 2007.

Research output: Contribution to journalArticle

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