Detection of a new deleterious SGCE gene variant in Moroccan family with inherited myoclonus-dystonia

Chbel, F; Charroute, H; Boulouiz, R; Hamdaoui, H; Mossafa, H; Benrahma, H; Ouldim, K

Chbel, F (通讯作者)，Univ Hassan 2, Lab BioGeosci & Ingn Mat, Ecole Normale Super, Km 8 Route EL Jadida, Casablanca, Morocco.

CLINICAL CASE REPORTS, 2022; 10 (3):

Abstract

Myoclonus-dystonia (M-D) is a pleiotropic neuropsychiatric disorder with autosomal dominant mode of inheritance with variable severity and incomplete ......

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