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Clinical, biochemical and molecular analysis of two infants with familial chylomicronemia syndrome
Familial chylomicronemia syndrome (FCS) is a rare autosomal recessive disease due mainly to inherited deficiencies in the proteins or enzymes involved in the clearance of triglycerides from circulation. It usually happens in late childhood and adolescence, which can have serious consequences if misd...
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| Publicado no: | Lipids Health Dis |
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| Main Authors: | , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4859971/ https://ncbi.nlm.nih.gov/pubmed/27153815 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12944-016-0254-z |
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