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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...
| Autores principales: | , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2016
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4859971/ https://www.ncbi.nlm.nih.gov/pubmed/27153815 http://dx.doi.org/10.1186/s12944-016-0254-z |