Recessively inherited parkinsonism: effect of ATP13A2 mutations on the clinical and neuroimaging phenotype
Research output: Contribution to journal › Journal article › Research › peer-review
To determine clinical features and to identify changes in brain structure and function in compound heterozygous and heterozygous ATP13A2 mutation carriers.
| Original language | English |
|---|---|
| Journal | Archives of Neurology |
| Volume | 67 |
| Issue number | 11 |
| Pages (from-to) | 1357-63 |
| Number of pages | 7 |
| ISSN | 0003-9942 |
| DOIs | |
| Publication status | Published - 1 Nov 2010 |
- Aged, Brain, Brain Mapping, Color Perception, Discrimination (Psychology), Female, Genetic Predisposition to Disease, Heterozygote, Humans, Magnetic Resonance Imaging, Male, Middle Aged, Mutation, Nerve Degeneration, Olfactory Perception, Parkinsonian Disorders, Pedigree, Phenotype, Prospective Studies, Proton-Translocating ATPases
Research areas
ID: 33437617