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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Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2015
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4704478/
https://www.ncbi.nlm.nih.gov/pubmed/26783545
http://dx.doi.org/10.1002/acn3.263

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4704478/
https://www.ncbi.nlm.nih.gov/pubmed/26783545
http://dx.doi.org/10.1002/acn3.263

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