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23. Genetics of hypercholesterolamemia: the detection of mutations in the apolipoprotein B gene using denaturing gradient gel electrophoresis. Gaffney D; Reid JM; Vass K; Packard CJ Z Gastroenterol; 1996 Jun; 34 Suppl 3():19-20. PubMed ID: 8767449 [No Abstract] [Full Text] [Related]
24. Molecular genetics of familial hypercholesterolaemia in Norway. Leren TP; Tonstad S; Gundersen KE; Bakken KS; Rødningen OK; Sundvold H; Ose L; Berg K J Intern Med; 1997 Mar; 241(3):185-94. PubMed ID: 9104431 [TBL] [Abstract][Full Text] [Related]
25. I705 variant in the low denisty lipoprotein receptor gene has no effect on plasma cholesterol levels. Heath KE; Whittal RA; Miller GJ; Humphries S J Med Genet; 2000 Sep; 37(9):713-5. PubMed ID: 11182933 [No Abstract] [Full Text] [Related]
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30. A common missense mutation (C210G) in the LDL receptor gene among Norwegian familial hypercholesterolemia subjects. Sundvold H; Solberg K; Tonstad S; Rødningen OK; Ose L; Berg K; Leren TP Hum Mutat; 1996; 7(1):70-1. PubMed ID: 8664907 [No Abstract] [Full Text] [Related]
31. Clinical studies in a kindred with a kinetic LDL receptor mutation causing familial hypercholesterolemia. Bilheimer DW; East C; Grundy SM; Nora JJ Am J Med Genet; 1985 Nov; 22(3):593-8. PubMed ID: 4061492 [TBL] [Abstract][Full Text] [Related]
32. Genetic mutation screening for the low-density lipoprotein receptor. Luft FC J Mol Med (Berl); 2006 Mar; 84(3):183-4. PubMed ID: 16482443 [No Abstract] [Full Text] [Related]
33. A keen eye for risk. Ford TJ; Rocchiccioli P BMJ; 2018 Feb; 360():j5884. PubMed ID: 29419393 [No Abstract] [Full Text] [Related]
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36. No prescription for despair. Robinson A CMAJ; 1993 Sep; 149(5):639-43. PubMed ID: 8364820 [No Abstract] [Full Text] [Related]
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38. Identification of a mutation, N543H, in exon 11 of the low-density lipoprotein receptor gene in a French family with familial hypercholesterolemia. Tricot-Guerber F; Saint-Jore B; Valenti K; Foulon T; Bost M; Hadjian AJ Hum Mutat; 1995; 6(1):87-8. PubMed ID: 7550239 [No Abstract] [Full Text] [Related]
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