Analysis of a founder mutation in the TH gene in a cohort of greek patients with Parkinson's disease

Mov Disord. 2016 Nov;31(11):1753-1754. doi: 10.1002/mds.26807. Epub 2016 Sep 26.

Authors

Roser Pons¹, Kyriaki Kekou², Roubina Antonellou³, Maria Svingou², Emmanouel Kanavakis², Leonidas Stefanis³

Affiliations

¹ First Department of Pediatrics, Agia Sophia Children's Hospital, National and Kapodistrian University of Athens, Greece.
² Department of Medical Genetics, Agia Sophia Children's Hospital, National and Kapodistrian University of Athens, Greece.
³ Second Department of Neurology, Attikon University Hospital, National and Kapodistrian University of Athens, Athens, Greece.

PMID: 27666733
DOI: 10.1002/mds.26807

No abstract available

Publication types

Letter
Research Support, Non-U.S. Gov't

MeSH terms

Adult
Age of Onset
Cohort Studies
Female
Greece / epidemiology
Humans
Male
Middle Aged
Mutation
Parkinson Disease / epidemiology
Parkinson Disease / genetics*
Parkinson Disease / physiopathology*
Tyrosine 3-Monooxygenase / genetics*

Substances

Tyrosine 3-Monooxygenase