Chylomicronaemia--current diagnosis and future therapies.
Brahm AJ, Hegele RA.
Brahm AJ, et al.
Nat Rev Endocrinol. 2015 Jun;11(6):352-62. doi: 10.1038/nrendo.2015.26. Epub 2015 Mar 3.
Nat Rev Endocrinol. 2015.
PMID: 25732519
Review.
The first form is very rare monogenic early-onset chylomicronaemia, which presents in childhood or adolescence and is often caused by homozygous mutations in the gene encoding lipoprotein lipase (LPL), its cofactors apolipoprotein C-II or apolipoprotein A-V, the LPL chaper …
The first form is very rare monogenic early-onset chylomicronaemia, which presents in childhood or adolescence and is often caused by homozy …