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Glucocerebrosidase Mutations in Chinese Subjects from Taiwan with Sporadic Parkinson Disease
BACKGROUND: An association between glucocerebrosidase, the enzyme deficient in Gaucher disease, and the synucleinopathies has been suggested both by the development of parkinsonism in Gaucher probands and carriers, as well as by the presence of mutations in the gene for glucocerebrosidase (GBA) in d...
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| Autors principals: | , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2007
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1950300/ https://ncbi.nlm.nih.gov/pubmed/17462935 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ymgme.2007.03.004 |
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