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Corticobasal syndrome in a man with Gaucher disease type 1: Expansion of the understanding of the neurological spectrum
Gaucher disease (GD) is an autosomal recessive condition that results from a deficiency of the enzyme β-glucocerebrosidase. The increased risk of primary parkinsonism symptoms among individuals affected with GD and carriers for the disorder is well-documented in the literature. However, these risks...
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Elsevier
2018
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6198121/ https://www.ncbi.nlm.nih.gov/pubmed/30364808 http://dx.doi.org/10.1016/j.ymgmr.2018.10.001 |