Biallelic Parkin (PARK2) mutations can cause a bvFTD phenotype without clinically relevant parkinsonism.

Zimmermann, Milan

Biallelic Parkin (PARK2) mutations can cause a bvFTD phenotype without clinically relevant parkinsonism. [electronic resource] - Parkinsonism & related disorders 10 2018 - 145-147 p. digital

Publication Type: Case Reports; Letter; Research Support, Non-U.S. Gov't

1873-5126

10.1016/j.parkreldis.2018.06.006 doi


Fluorodeoxyglucose F18--pharmacokinetics
Humans
Male
Middle Aged
Mutation--genetics
Parkinsonian Disorders--diagnostic imaging
Phenotype
Positron-Emission Tomography
Ubiquitin-Protein Ligases--genetics