Screening for SGCE mutations in Moroccan sporadic patients with Myoclonus-Dystonia syndrome

Rachad, L; El Otmani, H; Karkar, A; El Moutawakil, B; El Kadmiri, N; Nadifi, S

Rachad, L (reprint author), Hassan II Univ Casablanca, Fac Med & Pharm, Lab Med Genet & Mol Pathol, BP 9154, Casablanca, Morocco.

NEUROSCIENCE LETTERS, 2019; 703 (): 1

Abstract

Myoclonus-Dystonia (M-D) is a rare autosomal-dominant movement disorder characterized by myoclonic jerks in combination with dystonia and psychiatric ......

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