Genetics and Epigenetics of Parkinson's Disease
In 1997 a mutation in the a-synuclein (SNCA) gene was associated with familial autosomal dominant Parkinson’s disease (PD). Since then, several loci (PARK1-15) and genes have been linked to familial forms of the disease. There is now sufficient evidence that six of the so far identified genes at PAR...
Saved in:
Main Author: | Fabio Coppedè |
---|---|
Format: | Article |
Language: | English |
Published: |
Wiley
2012-01-01
|
Series: | The Scientific World Journal |
Online Access: | http://dx.doi.org/10.1100/2012/489830 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Genetic/Epigenetic Modulation, Ocular Diseases, and Therapeutic Prospective
by: Jingsheng Tuo, et al.
Published: (2013-01-01) -
Editorial: Genetics and epigenetics in ovarian aging
by: Honey V. Reddi
Published: (2025-02-01) -
Interplay between Epigenetics and Genetics in Cancer
by: Jae Duk Choi, et al.
Published: (2013-12-01) -
Genetic Rat Models of Parkinson's Disease
by: Ryan M. Welchko, et al.
Published: (2012-01-01) -
Cognitive Impairment in Genetic Parkinson’s Disease
by: A. Planas-Ballvé, et al.
Published: (2021-01-01)