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Cornea verticillata and acroparesthesia efficiently discriminate clusters of severity in Fabry disease
BACKGROUD: Fabry disease (OMIM #301 500), the most prevalent lysosomal storage disease, is caused by enzymatic defects in alpha-galactosidase A (GLA gene; Xq22.1). Fabry disease has historically been characterized by progressive renal failure, early stroke and hypertrophic cardiomyopathy, with a dim...
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| Gepubliceerd in: | PLoS One |
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| Hoofdauteurs: | , , , , , , , , , , , , , , , , , , , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Public Library of Science
2020
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7244174/ https://ncbi.nlm.nih.gov/pubmed/32442237 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0233460 |
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