Haplotype analysis of the human apolipoprotein B mutation associated with familial defective apolipoprotein B100
about
The roles of genetic polymorphisms and human immunodeficiency virus infection in lipid metabolismTwo amino acid substitutions in apolipoprotein B are in complete allelic association with the antigen group (x/y) polymorphism: evidence for little recombination in the 3' end of the human gene.Familial ligand-defective apolipoprotein B. Identification of a new mutation that decreases LDL receptor binding affinity.Complete paternal isodisomy for chromosome 8 unmasked by lipoprotein lipase deficiency.
P2860
Haplotype analysis of the human apolipoprotein B mutation associated with familial defective apolipoprotein B100
description
1990 nî lūn-bûn
@nan
1990 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1990 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
1990年の論文
@ja
1990年論文
@yue
1990年論文
@zh-hant
1990年論文
@zh-hk
1990年論文
@zh-mo
1990年論文
@zh-tw
1990年论文
@wuu
name
Haplotype analysis of the huma ...... defective apolipoprotein B100
@ast
Haplotype analysis of the huma ...... defective apolipoprotein B100
@en
type
label
Haplotype analysis of the huma ...... defective apolipoprotein B100
@ast
Haplotype analysis of the huma ...... defective apolipoprotein B100
@en
prefLabel
Haplotype analysis of the huma ...... defective apolipoprotein B100
@ast
Haplotype analysis of the huma ...... defective apolipoprotein B100
@en
P2860
P1476
Haplotype analysis of the huma ...... defective apolipoprotein B100
@en
P2093
B J McCarthy
E H Ludwig
P2860
P304
P407
P577
1990-10-01T00:00:00Z