P.378A complex movement disorder associated with myasthenic features: a novel phenotype caused by a homozygous NGLY1 mutation
D. Jacquier(University of Lausanne), Andrea Klein(University Children's Hospital Zurich), E. Roulet-Perez(University of Lausanne), Andrea Superti‐Furga(University of Lausanne), Thierry Küntzer(University of Lausanne), Jean‐Marc Good, B. Laubscher, David Mercati(University of Siena), Lauréane Mittaz‐Crettol(University of Lausanne), H. Fostad(University of Lausanne), Béryl Royer‐Bertrand(University of Lausanne)
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