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Molecular pathways in dystonia

The hereditary dystonias comprise a set of diseases defined by a common constellation of motor deficits. These disorders are most likely associated with different molecular etiologies, many of which have yet to be elucidated. Here we discuss recent advances in three forms of hereditary dystonia, DYT...

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Main Authors: Bragg, D. Cristopher, Armata, Ioanna A., Nery, Flavia C., Breakefield, Xandra O., Sharma, Nutan
格式: Artigo
語言:Inglês
出版: 2010
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在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC3073693/
https://ncbi.nlm.nih.gov/pubmed/21134457
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nbd.2010.11.015
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