Familial writer's cramp: a clinical clue for inherited coenzyme Q<sub>10</sub> deficiency.

Authors:
Amprosi M; Zech M; Steiger R; Nachbauer W; Eigentler A and 4 more

Journal:
Neurogenetics

Publication Year: 2020

DOI:
10.1007/s10048-020-00624-3

PMCID:
PMC7997836

PMID:
32830305

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Journal Information

Full Title: Neurogenetics

Abbreviation: Neurogenetics

Country: Unknown

Publisher: Unknown

Language: N/A

Publication Details

Subject Category: Neurology

Available in Europe PMC: Yes

Available in PMC: Yes

PDF Available: No

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"Conflicts of interest The authors declare that they have no conflict of interest."

Evidence found in paper:

"Funding information Open access funding provided by University of Innsbruck and Medical University of Innsbruck. Matthias Amprosi was supported by the grant I-3352-B28 from “Der Fonds zur Förderung der wissenschaftlichen Forschung (FWF)”."

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Last Updated: Aug 05, 2025