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  • RAB39B mutations are a rare fi...
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RAB39B mutations are a rare finding in Parkinson disease patients

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Bibliographic Details
Published inParkinsonism & related disorders Vol. 23; pp. 116 - 117
Main Authors Löchte, Tobias, Brüggemann, Norbert, Vollstedt, Eva-Juliane, Krause, Patricia, Domingo, Aloysius, Rosales, Raymond, Lee, Lillian V., Hopfner, Franziska, Westenberger, Ana, Kühn, Andrea, Klein, Christine, Lohmann, Katja
Format Journal Article
LanguageEnglish
Published England Elsevier Ltd 01.02.2016
Subjects
Aged
DNA Mutational Analysis
Female
Genetic Predisposition to Disease - genetics
Humans
Male
Middle Aged
Mutation
Neurology
Parkinson disease
Parkinson Disease - genetics
rab GTP-Binding Proteins - genetics
RAB39B
Variant
X-linked
Variant
Parkinson disease
X-linked
RAB39B
Online AccessGet full text
ISSN1353-8020
1873-5126
1873-5126
DOI10.1016/j.parkreldis.2015.12.014

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Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Correspondence-1
content type line 23
ISSN:1353-8020
1873-5126
1873-5126
DOI:10.1016/j.parkreldis.2015.12.014
  • ikona citování Cite this
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