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Parkinsonism Relat Disord. 2016 Feb;23:116-7. doi: 10.1016/j.parkreldis.2015.12.014. Epub 2015 Dec 22.

RAB39B mutations are a rare finding in Parkinson disease patients.

Author information

1
Institute of Neurogenetics, University of Luebeck, 23538 Luebeck, Germany.
2
Institute of Neurogenetics, University of Luebeck, 23538 Luebeck, Germany; Department of Neurology, University of Luebeck, 23538 Luebeck, Germany.
3
Institute of Neurogenetics, University of Luebeck, 23538 Luebeck, Germany; Department of Psychiatry, University of Luebeck, 23538 Luebeck, Germany.
4
Department of Neurology, Charité, University Medicine Berlin, 13353 Berlin, Germany.
5
Institute of Neurogenetics, University of Luebeck, 23538 Luebeck, Germany; XDP Study Group, Philippine Children's Medical Center, Quezon City, Philippines.
6
Faculty of Neurology and Psychiatry, University of Santo Tomas, Manila, Philippines.
7
XDP Study Group, Philippine Children's Medical Center, Quezon City, Philippines.
8
Department of Neurology, Christian Albrechts University, 24105 Kiel, Germany.
9
Institute of Neurogenetics, University of Luebeck, 23538 Luebeck, Germany. Electronic address: katja.lohmann@neuro.uni-luebeck.de.

KEYWORDS:

Parkinson disease; RAB39B; Variant; X-linked

[Indexed for MEDLINE]

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