Authors:
Rabes, JP
Varret, M
Devillers, M
Aegerter, P
Villeger, L
Krempf, M
Junien, C
Boileau, C
Citation: Jp. Rabes et al., R3531C mutation in the apolipoprotein B gene is not sufficient to cause hypercholesterolemia, ART THROM V, 20(10), 2000, pp. E76-E82
Authors:
Saint-Jore, B
Varret, M
Dachet, C
Rabes, JP
Devillers, M
Erlich, D
Blanchard, P
Krempf, M
Mathe, D
Chanu, B
Jacotot, B
Farnier, M
Bonaiti-Pellie, C
Junien, C
Boileau, C
Citation: B. Saint-jore et al., Autosomal dominant type IIa hypercholesterolemia: evaluation of the respective contributions of LDLR and APOB gene defects as well as a third major group of defects, EUR J HUM G, 8(8), 2000, pp. 621-630
Authors:
Thiart, R
Varret, M
Lintott, CJ
Scott, RS
Loubser, O
du Plessis, L
de Villiers, JNP
Boileau, C
Kotze, MJ
Citation: R. Thiart et al., Mutation analysis in a small cohort of New Zealand patients originating from the United Kingdom demonstrates genetic heterogeneity in familial hypercholesterolemia, MOL CELL PR, 14(5), 2000, pp. 299-304
Authors:
Varret, M
Rabes, JP
Saint-Jore, B
Cenarro, A
Marinoni, JC
Civeira, F
Devillers, M
Krempf, M
Coulon, M
Thiart, R
Kotze, MJ
Schmidt, H
Buzzi, JC
Kostner, GM
Bertolini, S
Pocovi, M
Rosa, A
Farnier, M
Martinez, M
Junien, C
Boileau, C
Citation: M. Varret et al., A third major locus for autosomal dominant hypercholesterolemia maps to 1p34.1-p32, AM J HU GEN, 64(5), 1999, pp. 1378-1387