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Altered Gene Expression in Prefrontal Cortex of a Fabry Disease Mouse Model
Fabry disease is an X-chromosome linked hereditary disease that is caused by loss of function mutations in the α-galactosidase A (α-Gal A) gene, resulting in defective glycolipid degradation and subsequent accumulation of globotriaosylceramide (Gb3) in different tissues, including vascular endotheli...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6036252/ https://www.ncbi.nlm.nih.gov/pubmed/30013462 http://dx.doi.org/10.3389/fnmol.2018.00201 |