Variable phenotypic expression in families with early-onset Parkinsonism due to PRKN mutations

J Neurol. 2014 Jun;261(6):1223-6. doi: 10.1007/s00415-014-7360-5. Epub 2014 Apr 30.

Authors

Siamak Karkheiran¹, Catharine E Krebs, Hossein Darvish, Mojgan Asadian, Gholam Ali Shahidi, Coro Paisán-Ruiz

Affiliation

¹ Movement Disorders Clinic, Hazrat Rasool Hospital, Tehran University of Medical Sciences, Tehran, Iran.

PMID: 24781841
DOI: 10.1007/s00415-014-7360-5

No abstract available

Publication types

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

MeSH terms

Adult
Family Health
Humans
Male
Middle Aged
Mutation / genetics*
Parkinsonian Disorders / genetics*
Phenotype
Ubiquitin-Protein Ligases / genetics*

Substances

Ubiquitin-Protein Ligases
parkin protein