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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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Détails bibliographiques
Auteurs principaux: Bragg, D. Cristopher, Armata, Ioanna A., Nery, Flavia C., Breakefield, Xandra O., Sharma, Nutan
Format: Artigo
Langue:Inglês
Publié: 2010
Sujets:
Accès en ligne: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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