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Characteristics of neurological Wilson’s disease with corpus callosum abnormalities
BACKGROUND: Wilson’s disease (WD) is an autosomal recessive disease of impaired copper metabolism. Previous study demonstrated that WD with corpus callosum abnormalities (WD-CCA) was limited to the posterior part (splenium). This study aimed to compare clinical features between WD-CCA and WD without...
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| Publicat a: | BMC Neurol |
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| Autors principals: | , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6499990/ https://ncbi.nlm.nih.gov/pubmed/31053106 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12883-019-1313-7 |
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