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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發表在:Ann Clin Transl Neurol
Main Authors: 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.
格式: Artigo
語言:Inglês
出版: John Wiley and Sons Inc. 2015
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Research Articles
在線閱讀: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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