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Vestibular and Saccadic Abnormalities in Gaucher’s Disease
Gaucher’s disease (GD) is a hereditary lysosomal storage disease characterized by abnormal deposition of glucocerebroside due to the enzyme glucocerebrosidase deficiency, resulting in multi-organ pathology. GD type III has a progressive neurological involvement. We studied the vestibular and saccadi...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer Berlin Heidelberg
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4110333/ https://ncbi.nlm.nih.gov/pubmed/24142279 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/8904_2013_264 |
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