Identification of deletions in the human low density lipoprotein receptor gene.

Author:

Horsthemke B,Dunning A,Humphries S

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference18 articles.

1. Expression of the familial hypercholesterolaemia gene in heterozygotes. Mechanisms for a dominant disorder in man;Brown, M.S.; Goldstein, J.L.;Science,1974

2. Familial hypercholesterolaemia. Defective binding of lipoproteins to cultured fibroblasts associated with impaired regulation of 3-hydroxy-3-methylglutaryl coenzyme A reductase activity;Brown, M.S.; Goldstein, J.L.;Proc Natl Acad Sci USA,1974

3. Familial hypercholesterolaemia, a genetic and metabolic study;Harlan, W.R.; Graham, J.B.; Estes, E.H.;Medicine (Baltimore),1966

4. Hyperlipidaemia in coronary heart disease. Part 2. Genetic analysis of lipid levels in 176 families and delineation of a new inherited disorder, combined hyperlipidaemia);Goldstein, J.L.; Schrott, H.G.; Hazzard, W.R.; Bierman, E.L.; Motulsky, A.G.;J Clin Invest,1973

5. The familial hyperlipoproteinaemias;Frederickson, D.S.; Goldstein, J.L.; Brown, M.S.,1978

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