Apolipoprotein B gene mutations in Austrian subjects with heart disease and their kindred

scientific article published on 01 March 1991

Apolipoprotein B gene mutations in Austrian subjects with heart disease and their kindred is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1161/01.ATV.11.2.371
P698PubMed publication ID1671822

P2093author name stringT L Innerarity
B J McCarthy
B Paulweber
F Sandhofer
M E Balestra
W Friedl
E H Ludwig
K S Arnold
P433issue2
P921main subjectheart diseaseQ190805
P304page(s)371-378
P577publication date1991-03-01
P1433published inArteriosclerosis and thrombosis : a journal of vascular biologyQ27709770
P1476titleApolipoprotein B gene mutations in Austrian subjects with heart disease and their kindred
P478volume11

Reverse relations

cites work (P2860)
Q70670394Absence of familial defective apolipoprotein B-100 in Israeli patients with dominantly inherited hypercholesterolemia and in offspring with parental history of myocardial infarction
Q33910296Accumulation of "small dense" low density lipoproteins (LDL) in a homozygous patients with familial defective apolipoprotein B-100 results from heterogenous interaction of LDL subfractions with the LDL receptor
Q36186468Familial defective apolipoprotein B-100: a common cause of primary hypercholesterolemia
Q68211354Familial defective apolipoprotein B100: clinical characteristics of 54 cases
Q35553545Familial ligand-defective apolipoprotein B. Identification of a new mutation that decreases LDL receptor binding affinity
Q53393462First International Workshop on Familial Defective apo B-100, Munich, November 1991
Q51576650Statin therapy in a kindred with both apolipoprotein B and low density lipoprotein receptor gene defects.

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