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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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Autores principales: Bragg, D. Cristopher, Armata, Ioanna A., Nery, Flavia C., Breakefield, Xandra O., Sharma, Nutan
Formato: Artigo
Lenguaje:Inglês
Publicado: 2010
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Acceso en línea: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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