Recessive mutations in VPS13D cause childhood ‐onset movement disorders

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Source: Annals of Neurology - March 8, 2018 Category: Neurology Authors: Julie Gauthier, Inge A. Meijer, Davor Lessel, Niccol ò E. Mencacci, Dimitri Krainc, Maja Hempel, Konstantinos Tsiakas, Holger Prokisch, Elsa Rossignol, Margaret H. Helm, Lance H. Rodan, Jason Karamchandani, Miryam Carecchio, Steven J. Lubbe, Aida Telegra Tags: Brief Communication Source Type: research