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NEW EMBO MEMBER’S REVIEW: Molecular background of progressive myoclonus epilepsy
Research on human inherited diseases provides a powerful tool to identify an intrinsically important subset of genes vital to healthy functioning of the organism. Progressive myoclonus epilepsies (PMEs) are a group of rare inherited disorders characterized by the association of epilepsy, myoclonus a...
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| Natura: | Artigo |
| Lingua: | Inglês |
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Oxford University Press
2003
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| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC165608/ https://ncbi.nlm.nih.gov/pubmed/12853462 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/emboj/cdg338 |
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