Phenotypic variation in patients heterozygous for familial defective apolipoprotein B (FDB) in three European countries.
about
Mechanisms and genetic determinants regulating sterol absorption, circulating LDL levels, and sterol elimination: implications for classification and disease riskThe roles of genetic polymorphisms and human immunodeficiency virus infection in lipid metabolismRapid detection of 3500Q and 3531 mutations and MspI polymorphism in exon 26 at the apolipoprotein B gene.Familial hypercholesterolemia and response to statin therapy according to LDLR genetic background.Familial defective apolipoprotein B-100 and increased low-density lipoprotein cholesterol and coronary artery calcification in the old order amish.Genetic heterogeneity of autosomal dominant hypercholesterolemia.Impact of genetic defects on atherosclerosis in patients suspected of familial hypercholesterolaemia.
P2860
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P2860
Phenotypic variation in patients heterozygous for familial defective apolipoprotein B (FDB) in three European countries.
description
1997 nî lūn-bûn
@nan
1997年の論文
@ja
1997年学术文章
@wuu
1997年学术文章
@zh
1997年学术文章
@zh-cn
1997年学术文章
@zh-hans
1997年学术文章
@zh-my
1997年学术文章
@zh-sg
1997年學術文章
@yue
1997年學術文章
@zh-hant
name
Phenotypic variation in patien ...... ) in three European countries.
@en
Phenotypic variation in patients heterozygous for familial defective apolipoprotein B
@nl
type
label
Phenotypic variation in patien ...... ) in three European countries.
@en
Phenotypic variation in patients heterozygous for familial defective apolipoprotein B
@nl
prefLabel
Phenotypic variation in patien ...... ) in three European countries.
@en
Phenotypic variation in patients heterozygous for familial defective apolipoprotein B
@nl
P2093
P356
P1476
Phenotypic variation in patien ...... ) in three European countries.
@en
P2093
Defesche JC
Faergeman O
Kastelein JJ
Klausen IC
P304
P356
10.1161/01.ATV.17.4.741
P407
P577
1997-04-01T00:00:00Z