about
Molecular and functional analysis of two new MTTP gene mutations in an atypical case of abetalipoproteinemiaLiving the PCSK9 adventure: from the identification of a new gene in familial hypercholesterolemia towards a potential new class of anticholesterol drugs.Genetic diagnosis of familial hypercholesterolaemia by targeted next-generation sequencing.Decreased APOE-containing HDL subfractions and cholesterol efflux capacity of serum in mice lacking Pcsk9.New technologies for delineating and characterizing the lipid exome: prospects for understanding familial combined hyperlipidemia.A new method for measurement of total plasma PCSK9: clinical applications.The genetics of familial combined hyperlipidaemia.Progress in the care of common inherited atherogenic disorders of apolipoprotein B metabolism.
P2860
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P2860
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年学术文章
@wuu
2008年学术文章
@zh
2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
@yue
2008年學術文章
@zh-hant
name
A PCSK9 variant and familial combined hyperlipidaemia.
@en
A PCSK9 variant and familial combined hyperlipidaemia.
@nl
type
label
A PCSK9 variant and familial combined hyperlipidaemia.
@en
A PCSK9 variant and familial combined hyperlipidaemia.
@nl
prefLabel
A PCSK9 variant and familial combined hyperlipidaemia.
@en
A PCSK9 variant and familial combined hyperlipidaemia.
@nl
P2093
P50
P356
P1476
A PCSK9 variant and familial combined hyperlipidaemia
@en
P2093
J Davignon
M Abifadel
M Devillers
P304
P356
10.1136/JMG.2008.059980
P407
P577
2008-08-15T00:00:00Z