Screening for SGCE mutations in Moroccan sporadic patients with Myoclonus-Dystonia syndrome-Reference-Cited by-同舟云学术

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

Published:2019-06 Issue: Volume:703 Page:1-4
ISSN:0304-3940
Container-title:Neuroscience Letters
language:en
Short-container-title:Neuroscience Letters

Author:

Rachad Laila,El Otmani Hicham,Karkar Adnane^ORCID,El Moutawakil Bouchra,El Kadmiri Nadia,Nadifi Sellama

Publisher

Elsevier BV

Subject

General Neuroscience

Reference21 articles.

1. H. Sarva, J. Miravite, M.C. Swan, A. Deik, D. Raymond, W.L. Severt, B.H. Kopell, A Case of Myoclonus–Dystonia Responding to Low-frequency Pallidal Stimulation, (n.d.) 3.

2. Genetic aspects of myoclonus–dystonia syndrome (MDS);Rachad;Mol. Neurobiol.,2017

3. Myoclonus-dystonia syndrome: case report;Oguz Akarsu;North Clin. Istanb.,2015

4. Hereditary essential myoclonus;Mahloudji;Brain J. Neurol.,1967

5. Psychiatric symptoms in myoclonus-dystonia syndrome are just concomitant features regardless of the SGCE gene mutation;Kim;Parkinsonism Relat. Disord.,2017

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Detection of a new deleterious SGCE gene variant in Moroccan family with inherited myoclonus–dystonia;Clinical Case Reports;2022-03

2. Population Prevalence of Deleterious SGCE Variants;Tremor and Other Hyperkinetic Movements;2020-11-04

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