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Publication
PropertyValue
Working Groups Klopstock
SubprojectNone
Open AccessOpen Access Yes
Publication TypeJournal Article
Peer ReviewedYes
PMIDPubMed ID 28459997
DOIDOI 10.1093/brain/awx095
Publication Year2017
TitleHypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia. Wikidata
JournalBrain : a journal of neurology
ISSN0006-8950
ESSN1460-2156
URL https://www.ncbi.nlm.nih.gov/pubmed/?term=28459997%5Buid%5D
Pages1561-1578
Issue6
Volume140
Journal AbbreviationBrain
AuthorsMinnerop M, Kurzwelly D, Wagner H, Soehn AS, Reichbauer J, Tao F, Rattay TW, Peitz M, Rehbach K, Giorgetti A, Pyle A, Thiele H, Altmüller J, Timmann D, Karaca I, Lennarz M, Baets J, Hengel H, Synofzik M, Atasu B, Feely S, Kennerson M, Stendel C, Lindig T, Gonzalez MA, Stirnberg R, Sturm M, Roeske S, Jung J, Bauer P, Lohmann E, Herms S, Heilmann-Heimbach S, Nicholson G, Mahanjah M, Sharkia R, Carloni P, Brüstle O, Klopstock T, Mathews KD, Shy ME, de Jonghe P, Chinnery PF, Horvath R, Kohlhase J, Schmitt I, Wolf M, Greschus S, Amunts K, Maier W, Schöls L, Nürnberg P, Zuchner S, Klockgether T, Ramirez A, Schüle R
First AuthorMinnerop M
Last AuthorSchüle R
ScholiaScholia Wikidata-based representation at Scholia

 External Resources

 Q50240123  Wikidata ID