Compound Heterozygous DARS2 Mutations as a Mimic of Hereditary Spastic Paraplegia

Martje G. Pauly, Yorck Hellenbroich, Kathrin Grundmann-Hauser, Frauke Hinrichs, Katja Lohmann, Norbert Brüggemann*

*Korrespondierende/r Autor/-in für diese Arbeit
3 Zitate (Scopus)
OriginalspracheEnglisch
ZeitschriftMovement Disorders Clinical Practice
Jahrgang8
Ausgabenummer6
Seiten (von - bis)972-976
Seitenumfang5
DOIs
PublikationsstatusVeröffentlicht - 08.2021

Fördermittel

The study was supported by the German Research Foundation (FOR2488), the German Research Foundation via the Clinician Scientist School Lübeck (DFG‐GEPRIS 413535489), and the Damp Foundation. The authors do not declare any conflicts of interest or competing interests. Martje G. Pauly is funded by the Clinician Scientist School Lübeck. Yorck Hellenbroich has nothing to report. Kathrin Grundmann‐Hauser has nothing to report. Frauke Hinrichs has nothing to report. Katja Lohmann received research funding from the German Research Foundation, the Damp‐Stiftung and the Movement Disorders Society and is member of the GP2 initiative within ASAP ( https://parkinsonsroadmap.org/gp2/ ). Norbert Brüggemann served as a consultant for Censa Pharmaceuticals, Centogene, and Bridgebio and is funded by the German Research Foundation (BR4328.2‐1, GRK1957).

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