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Clinical characteristics and plasma lipids in subjects with familial combined hypolipidemia: a pooled analysis
Angiopoietin-like 3 (ANGPTL3) regulates lipoprotein metabolism by modulating extracellular lipases. Loss-of function mutations in ANGPTL3 gene cause familial combined hypolipidemia (FHBL2). The mode of inheritance and hepatic and vascular consequences of FHBL2 have not been fully elucidated. To get...
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| Autori principali: | , , , , , , , , , , , , , , , , , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
The American Society for Biochemistry and Molecular Biology
2013
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3826694/ https://ncbi.nlm.nih.gov/pubmed/24058201 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1194/jlr.P039875 |
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