Familial Parkinsonism and early onset Parkinson's disease in a Brazilian Movement Disorders clinic: Phenotypic characterization and frequency of SNCA, PRKN, PINK1 and LRRK2 mutations

The aim of the study was to evaluate the frequency and to perform phenotypic and genotypic characterization of familial Parkinsonism and early onset Parkinson's disease (EOPD) in a Brazilian movement disorder unit. We performed a standardized clinical assessment of patients followed by sequenci...

Celý popis

Uloženo v:
Podrobná bibliografie
Hlavní autoři: Camargos, Sarah Teixeira, Dornas, Leonardo Oliveira, Momeni, Parastoo, Lees, Andrew, Hardy, John, Singleton, Andrew, Cardoso, Francisco
Médium: Artigo
Jazyk:Inglês
Vydáno: 2009
Témata:
Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC2850048/
https://ncbi.nlm.nih.gov/pubmed/19205068
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mds.22365
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!

Podobné jednotky