Compound Heterozygous DARS2 Mutations as a Mimic of Hereditary Spastic Paraplegia

TY - JOUR

T1 - Compound Heterozygous DARS2 Mutations as a Mimic of Hereditary Spastic Paraplegia

AU - Pauly, Martje G.

AU - Hellenbroich, Yorck

AU - Grundmann-Hauser, Kathrin

AU - Hinrichs, Frauke

AU - Lohmann, Katja

AU - Brüggemann, Norbert

N1 - Funding Information: 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. Funding Information: 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).

PY - 2021/8

Y1 - 2021/8

UR - https://www.scopus.com/pages/publications/85107785768

UR - https://www.mendeley.com/catalogue/4a2df11e-24f6-3c98-97bd-02a8bda28433/

U2 - 10.1002/mdc3.13258

DO - 10.1002/mdc3.13258

M3 - Journal articles

C2 - 34405109

AN - SCOPUS:85107785768

SN - 2330-1619

VL - 8

SP - 972

EP - 976

JO - Movement Disorders Clinical Practice

JF - Movement Disorders Clinical Practice

IS - 6

ER -