POLR3A variants with striatal involvement and extrapyramidal movement disorder.

Authors:
Harting I; Al-Saady M; Krägeloh-Mann I; Bley A; Hempel M and 12 more

Journal:
Neurogenetics

Publication Year: 2020

DOI:
10.1007/s10048-019-00602-4

PMCID:
PMC7064625

PMID:
31940116

View on PubMed View on PMC View Publisher
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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"Conflict of interest All authors declare no conflicts of interest in the publication of this manuscript."

Evidence found in paper:

"Funding information AP was supported by the Centre for Biomedical Research on Rare Diseases (CIBERER), the URDCat program (PERIS SLT002/16/00174), the Hesperia Foundation, ‘La Marató de TV3’ Foundation 345/C/2014, and the Secretariat for Universities and Research of the Ministry of Business and Knowledge of the Government of Catalonia [2017SG R1206]."

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