Altered Gene Expression in Prefrontal Cortex of a Fabry Disease Mouse Model
Altered Gene Expression in Prefrontal Cortex of a Fabry Disease Mouse Model
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Switzerland: Frontiers Research Foundation
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Language
English
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Switzerland: Frontiers Research Foundation
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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 endothelial cells and neurons in the peripheral and central...
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Altered Gene Expression in Prefrontal Cortex of a Fabry Disease Mouse Model
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TN_cdi_doaj_primary_oai_doaj_org_article_9dc4f97a6f4a452dae4370f3a5fd24df
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_9dc4f97a6f4a452dae4370f3a5fd24df
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ISSN
1662-5099
E-ISSN
1662-5099
DOI
10.3389/fnmol.2018.00201
