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Genetics of Neurodegeneration with Brain Iron Accumulation
The condition originally called Hallervorden-Spatz syndrome is a collection of related disorders involving abnormal iron accumulation in the basal ganglia, usually manifesting with a movement disorder. To date, mutations in the following genes have been associated with neurodegeneration with brain i...
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| Gepubliceerd in: | Curr Neurol Neurosci Rep |
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| Hoofdauteurs: | , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
2011
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5908240/ https://ncbi.nlm.nih.gov/pubmed/21286947 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s11910-011-0181-3 |
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