Analyses of familial chylomicronemia syndrome in Pereira, Colombia 2010–2020: a cross-sectional study
Abstract Background and aim Familial chylomicronemia syndrome (FCS) is a rare autosomal recessive metabolic disorder caused by mutations in genes involved in chylomicron metabolism. On the other hand, multifactorial chylomicronemia syndrome (MCS) is a polygenic disorder and the most frequent cause o...
Hlavní autoři: | , , , , |
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Médium: | Článek |
Jazyk: | English |
Vydáno: |
BMC
2023-03-01
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Edice: | Lipids in Health and Disease |
Témata: | |
On-line přístup: | https://doi.org/10.1186/s12944-022-01768-x |