Recessively inherited parkinsonism: effect of ATP13A2 mutations on the clinical and neuroimaging phenotype
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
To determine clinical features and to identify changes in brain structure and function in compound heterozygous and heterozygous ATP13A2 mutation carriers.
Originalsprog | Engelsk |
---|---|
Tidsskrift | Archives of Neurology |
Vol/bind | 67 |
Udgave nummer | 11 |
Sider (fra-til) | 1357-63 |
Antal sider | 7 |
ISSN | 0003-9942 |
DOI | |
Status | Udgivet - 1 nov. 2010 |
ID: 33437617