A novel SGCE gene mutation in a Moroccan sporadic case with myoclonus-dystonia syndrome

Rachad, L; El Otmani, H; Karkar, A; 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.

GENE REPORTS, 2018; 11 (): 121

Abstract

Inherited myoclonus-dystonia syndrome (MDS) is a rare autosomal-dominant movement disorder characterized by myoclonic jerks and dystonia accompanied w......

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