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Affective and cognitive behavior in the alpha-galactosidase A deficient mouse model of Fabry disease
Fabry disease is an X-linked inherited lysosomal storage disorder with intracellular accumulation of globotriaosylceramide (Gb3) due to α-galactosidase A (α-Gal A) deficiency. Fabry patients frequently report of anxiety, depression, and impaired cognitive function. We characterized affective and cog...
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| Publicado no: | PLoS One |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Public Library of Science
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5491260/ https://ncbi.nlm.nih.gov/pubmed/28662189 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0180601 |
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