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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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Bragg, D. Cristopher, Armata, Ioanna A., Nery, Flavia C., Breakefield, Xandra O., Sharma, Nutan
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 2010
Gaiak:
Sarrera elektronikoa: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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