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The burden of familial chylomicronemia syndrome in Canadian patients
BACKGROUND: Familial chylomicronemia syndrome (FCS) is a rare autosomal recessive disorder characterized by persistent extreme hypertriglyceridemia as a result of lipoprotein lipase deficiency. Canada is an important region for FCS research due to the high prevalence rates. The burden of illness and...
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| Publicat a: | Lipids Health Dis |
|---|---|
| Autors principals: | , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7268343/ https://ncbi.nlm.nih.gov/pubmed/32487261 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12944-020-01302-x |
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