Morbus Fabry and Parkinson's Disease—More Evidence for a Possible Genetic Link

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Veröffentlicht in:Movement disorders 2024-02, Vol.39 (2), p.449-451
Hauptverfasser: Müller, Susanne, Kassubek, Jan, Hold, Stephan T., Kasper, David C., Mayer, Benjamin, Müller, Kathrin, Freischmidt, Axel, Siebert, Reiner, Braak, Heiko, Ludolph, Albert C., Del Tredici, Kelly
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container_end_page 451
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container_title Movement disorders
container_volume 39
creator Müller, Susanne
Kassubek, Jan
Hold, Stephan T.
Kasper, David C.
Mayer, Benjamin
Müller, Kathrin
Freischmidt, Axel
Siebert, Reiner
Braak, Heiko
Ludolph, Albert C.
Del Tredici, Kelly
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doi_str_mv 10.1002/mds.29686
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subjects angiokeratoma diffuse
Fabry Disease - genetics
Fabry's disease
GLA deficiency
glycosphingolipids
Humans
Movement disorders
Mutation
Neurodegenerative diseases
Parkinson Disease - genetics
Parkinson's disease
α‐galactosidase a (aGal)
α‐galactosidase a (GLA) deficiency
title Morbus Fabry and Parkinson's Disease—More Evidence for a Possible Genetic Link
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