Article
Review: Familial Parkinson's disease--genetics, clinical phenotype and neuropathology in relation to the common sporadic form of the disease.
Neuropathology and applied neurobiology - 1 Jun 2008
Schiesling Carola, Kieper Nicole, Seidel Kay, Krüger Rejko
Abstract excerpt
The identification of the first gene in familial Parkinson's disease (PD) only 10 years ago was a major step in the understanding of the molecular mechanisms in neurodegeneration. Alpha-synuclein aggregation was not only recognized as a key event in neurodegeneration in patients carrying mutations in this gene, but it turned out to be the most consistent marker to define Lewy body pathology also in non-heritable...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
