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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Detalles Bibliográficos
Autores principales: Hofmann, Lukas, Karl, Franziska, Sommer, Claudia, Üçeyler, Nurcan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5491260/
https://www.ncbi.nlm.nih.gov/pubmed/28662189
http://dx.doi.org/10.1371/journal.pone.0180601

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5491260/
https://www.ncbi.nlm.nih.gov/pubmed/28662189
http://dx.doi.org/10.1371/journal.pone.0180601

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