Novel mutations of APOB cause ApoB truncations undetectable in plasma and familial hypobetalipoproteinemia.
about
Familial hypobetalipoproteinemia-induced nonalcoholic steatohepatitisMonogenic hypocholesterolaemic lipid disorders and apolipoprotein B metabolism.Insights from human congenital disorders of intestinal lipid metabolism.Abnormal apolipoprotein B pre-mRNA splicing in patients with familial hypobetalipoproteinaemia.Fatty liver in familial hypobetalipoproteinemia: triglyceride assembly into VLDL particles is affected by the extent of hepatic steatosis.Evidence for a quantitative trait locus affecting low levels of apolipoprotein B and low density lipoprotein on chromosome 10 in Caucasian families.
P2860
Novel mutations of APOB cause ApoB truncations undetectable in plasma and familial hypobetalipoproteinemia.
description
2002 nî lūn-bûn
@nan
2002年の論文
@ja
2002年学术文章
@wuu
2002年学术文章
@zh-cn
2002年学术文章
@zh-hans
2002年学术文章
@zh-my
2002年学术文章
@zh-sg
2002年學術文章
@yue
2002年學術文章
@zh
2002年學術文章
@zh-hant
name
Novel mutations of APOB cause ...... ilial hypobetalipoproteinemia.
@en
Novel mutations of APOB cause ...... ilial hypobetalipoproteinemia.
@nl
type
label
Novel mutations of APOB cause ...... ilial hypobetalipoproteinemia.
@en
Novel mutations of APOB cause ...... ilial hypobetalipoproteinemia.
@nl
prefLabel
Novel mutations of APOB cause ...... ilial hypobetalipoproteinemia.
@en
Novel mutations of APOB cause ...... ilial hypobetalipoproteinemia.
@nl
P2093
P2860
P356
P1433
P1476
Novel mutations of APOB cause ...... ilial hypobetalipoproteinemia.
@en
P2093
Daniela S Gerhard
Gustav Schonfeld
Rosalind J Neuman
William L Isley
William S Harris
P2860
P304
P356
10.1002/HUMU.10101
P577
2002-08-01T00:00:00Z