Psychiatric disorders, myoclonus dystonia and SGCE: an international study

OBJECTIVE: Myoclonus‐dystonia (M‐D) is a hyperkinetic movement disorder, typically alcohol‐responsive upper body myoclonus and dystonia. The majority of autosomal dominant familial cases are caused by epsilon‐sarcoglycan gene (SGCE) mutations. Previous publications have observed increased rates of p...

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Dades bibliogràfiques
Publicat a:Ann Clin Transl Neurol
Autors principals: Peall, Kathryn J., Dijk, Joke M., Saunders‐Pullman, Rachel, Dreissen, Yasmine E. M., van Loon, Ilke, Cath, Danielle, Kurian, Manju A., Owen, Michael J., Foncke, Elisabeth M. J., Morris, Huw R., Gasser, Thomas, Bressman, Susan, Asmus, Friedrich, Tijssen, Marina A. J.
Format: Artigo
Idioma:Inglês
Publicat: John Wiley and Sons Inc. 2015
Matèries:
Research Articles
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4704478/
https://ncbi.nlm.nih.gov/pubmed/26783545
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/acn3.263
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