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Machado-Joseph Disease: from first descriptions to new perspectives
Machado-Joseph Disease (MJD), also known as spinocerebellar ataxia type 3 (SCA3), represents the most common form of SCA worldwide. MJD is an autosomal dominant neurodegenerative disorder of late onset, involving predominantly the cerebellar, pyramidal, extrapyramidal, motor neuron and oculomotor sy...
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| Hauptverfasser: | , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
BioMed Central
2011
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3123549/ https://ncbi.nlm.nih.gov/pubmed/21635785 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1750-1172-6-35 |
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