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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: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2010
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| Assuntos: | |
| Acesso em linha: | 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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