Response to HMG CoA reductase inhibitors in heterozygous familial hypercholesterolemia due to the 10-kb deletion ("French Canadian mutation") of the LDL receptor gene

scientific article published on 01 August 1994

Response to HMG CoA reductase inhibitors in heterozygous familial hypercholesterolemia due to the 10-kb deletion ("French Canadian mutation") of the LDL receptor gene is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1161/01.ATV.14.8.1258
P698PubMed publication ID8049186

P50authorJean DavignonQ3171589
P2093author name stringS Qiu
J Genest
G Roederer
R Dufour
A Minnich
L Karayan
C Betard
P433issue8
P921main subjectheterozygosityQ124059385
familial hypercholesterolemiaQ2711291
P304page(s)1258-1263
P577publication date1994-08-01
P1433published inArteriosclerosis and thrombosis : a journal of vascular biologyQ27709770
P1476titleResponse to HMG CoA reductase inhibitors in heterozygous familial hypercholesterolemia due to the 10-kb deletion ("French Canadian mutation") of the LDL receptor gene
P478volume14

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cites work (P2860)
Q30670019A novel assay uncovers an unexpected role for SR-BI in LDL transcytosis.
Q72992412Familial hypercholesterolemia. Acceptor splice site (G-->C) mutation in intron 7 of the LDL-R gene: alternate RNA editing causes exon 8 skipping or a premature stop codon in exon 8. LDL-R(Honduras-1) [LDL-R1061(-1) G-->C]
Q74449552Influence of genotype at the low density lipoprotein (LDL) receptor gene locus on the clinical phenotype and response to lipid-lowering drug therapy in heterozygous familial hypercholesterolaemia. The Familial Hypercholesterolaemia Regression Study
Q36767518Mechanisms of disease: genetic causes of familial hypercholesterolemia
Q39923040The effects of rosuvastatin on the serum cortisol, serum lipid, and serum mevalonic acid levels in the healthy Indian male population

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