Characterization of six patients who are double heterozygotes for familial hypercholesterolemia and familial defective apo B-100.

scientific article published in July 1993

Characterization of six patients who are double heterozygotes for familial hypercholesterolemia and familial defective apo B-100. is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1161/01.ATV.13.7.1076
P698PubMed publication ID8318509

P2093author name stringD C Rubinsztein
F J Raal
G A Coetzee
D R van der Westhuyzen
H C Seftel
G Pilcher
P433issue7
P407language of work or nameEnglishQ1860
P921main subjecthypercholesterolemiaQ762713
familial hypercholesterolemiaQ2711291
P304page(s)1076-1081
P577publication date1993-07-01
P1433published inArteriosclerosis and thrombosis : a journal of vascular biologyQ27709770
P1476titleCharacterization of six patients who are double heterozygotes for familial hypercholesterolemia and familial defective apo B-100
P478volume13

Reverse relations

cites work (P2860)
Q41779360Familial hypercholesterolaemia
Q27003094Mechanisms and genetic determinants regulating sterol absorption, circulating LDL levels, and sterol elimination: implications for classification and disease risk
Q48130479New Sequencing technologies help revealing unexpected mutations in Autosomal Dominant Hypercholesterolemia.
Q46347224Simultaneous detection of multiple familial hypercholesterolemia mutations facilitates an improved diagnostic service in South african patients at high risk of cardiovascular disease
Q51576650Statin therapy in a kindred with both apolipoprotein B and low density lipoprotein receptor gene defects.
Q28214323Statins in homozygous familial hypercholesterolemia

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