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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...
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| Publicado no: | Front Mol Neurosci |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Frontiers Media S.A.
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6036252/ https://ncbi.nlm.nih.gov/pubmed/30013462 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fnmol.2018.00201 |
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