A missense mutation at codon 188 of the human lipoprotein lipase gene is a frequent cause of lipoprotein lipase deficiency in persons of different ancestries.

Lipoprotein lipase (LPL) plays a crucial role in the regulation of lipoprotein metabolism by hydrolysing the core triglycerides of circulating chylomicrons and VLDL. Human, bovine, mouse, and guinea pig complementary DNA clones have recently been isolated and the organization of the human LPL gene i...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Monsalve, M V, Henderson, H, Roederer, G, Julien, P, Deeb, S, Kastelein, J J, Peritz, L, Devlin, R, Bruin, T, Murthy, M R
Formato: Artigo
Idioma:Inglês
Publicado em: 1990
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC296787/
https://ncbi.nlm.nih.gov/pubmed/1975597
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados