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pro vyhledávání: '"Félicien MBou"'
Autor:
René Wintjens, Dominique Bozon, Khaldia Belabbas, Félicien MBou, Jean-Philippe Girardet, Patrick Tounian, Mathilde Jolly, Franck Boccara, Ariel Cohen, Alexandra Karsenty, Béatrice Dubern, Jean-Claude Carel, Ahlam Azar-Kolakez, François Feillet, François Labarthe, Anne-Marie Colin Gorsky, Alice Horovitz, Catherine Tamarindi, Pierre Kieffer, Anne Lienhardt, Olivier Lascols, Mathilde Di Filippo, Fabienne Dufernez
Publikováno v:
Journal of Lipid Research, Vol 57, Iss 3, Pp 482-491 (2016)
Autosomal dominant hypercholesterolemia (ADH) is a human disorder characterized phenotypically by isolated high-cholesterol levels. Mutations in the low density lipoprotein receptor (LDLR), APOB, and proprotein convertase subtilisin/kexin type 9 (PCS
Externí odkaz:
https://doaj.org/article/9302fb48e9784280aff06c74971d3e59
Autor:
Pierre Kieffer, Jean-Philippe Girardet, Khaldia Belabbas, Anne Lienhardt, Ahlam Azar-Kolakez, François Labarthe, Anne-Marie Colin Gorsky, Olivier Lascols, Béatrice Dubern, Franck Boccara, Catherine Tamarindi, Mathilde Di Filippo, Jean-Claude Carel, Félicien MBou, Alice Horovitz, René Wintjens, Dominique Bozon, Mathilde Jolly, Fabienne Dufernez, Ariel Cohen, François Feillet, Patrick Tounian, A. Karsenty
Publikováno v:
Journal of Lipid Research
Journal of Lipid Research, American Society for Biochemistry and Molecular Biology, 2016, 57 (3), pp.482-491. ⟨10.1194/jlr.P055699⟩
Journal of Lipid Research, 2016, 57 (3), pp.482-491. ⟨10.1194/jlr.P055699⟩
Journal of Lipid Research 3 (57), 482-491. (2016)
Journal of Lipid Research, Vol 57, Iss 3, Pp 482-491 (2016)
Journal of lipid research, 57 (3
Journal of Lipid Research, American Society for Biochemistry and Molecular Biology, 2016, 57 (3), pp.482-491. ⟨10.1194/jlr.P055699⟩
Journal of Lipid Research, 2016, 57 (3), pp.482-491. ⟨10.1194/jlr.P055699⟩
Journal of Lipid Research 3 (57), 482-491. (2016)
Journal of Lipid Research, Vol 57, Iss 3, Pp 482-491 (2016)
Journal of lipid research, 57 (3
Autosomal dominant hypercholesterolemia (ADH) is a human disorder characterized phenotypically by isolated high-cholesterol levels. Mutations in the low density lipoprotein receptor ( LDLR ), APOB, and proprotein convertase subtilisin/kexin type 9 (