The New p.F1700L LRRK2 Variant Causes Parkinson's Disease by Extensively Increasing Kinase Activity.

Borsche, Max; Pratuseviciute, Neringa; Schaake, Susen; Hinrichs, Frauke; Morel, Gabriel; Uter, Jan; Lohmann, Katja; Klein, Christine; Alessi, Dario R; Hagenah, Johann; Sammler, Esther

Borsche, Max; Pratuseviciute, Neringa; Schaake, Susen; Hinrichs, Frauke; Morel, Gabriel; Uter, Jan; Lohmann, Katja; Klein, Christine; Alessi, Dario R; Hagenah, Johann; Sammler, Esther.

Affiliation

Borsche M; Institute of Neurogenetics, University of Lübeck, Lübeck, Germany.
Pratuseviciute N; Department of Neurology, University of Lübeck, Lübeck, Germany.
Schaake S; MRC Protein Phosphorylation and Ubiquitylation Unit, School of Life Sciences, University of Dundee, Dundee, United Kingdom.
Hinrichs F; Institute of Neurogenetics, University of Lübeck, Lübeck, Germany.
Morel G; Institute of Neurogenetics, University of Lübeck, Lübeck, Germany.
Uter J; MRC Protein Phosphorylation and Ubiquitylation Unit, School of Life Sciences, University of Dundee, Dundee, United Kingdom.
Lohmann K; Institute of Neurogenetics, University of Lübeck, Lübeck, Germany.
Klein C; Department of Neurology, University of Lübeck, Lübeck, Germany.
Alessi DR; Institute of Neurogenetics, University of Lübeck, Lübeck, Germany.
Hagenah J; Institute of Neurogenetics, University of Lübeck, Lübeck, Germany.
Sammler E; MRC Protein Phosphorylation and Ubiquitylation Unit, School of Life Sciences, University of Dundee, Dundee, United Kingdom.

Mov Disord ; 38(6): 1105-1107, 2023 06.

Article in En | MEDLINE | ID: mdl-36971062

Subject(s)

Fulltext

Add to My VHL

XML

PubMed Links

Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Parkinson Disease Type of study: Etiology_studies Limits: Humans Language: En Journal: Mov Disord Journal subject: NEUROLOGIA Year: 2023 Document type: Article Affiliation country: Alemania

Fulltext

Add to My VHL

XML

PubMed Links

Search on Google