Après le récepteur des LDL et l'apolipoprotéine B, l'hypercholestérolémie familiale révèle son troisième protagoniste: PCSK9
Author:
Publisher
Elsevier BV
Subject
Endocrinology,General Medicine,Endocrinology, Diabetes and Metabolism
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3. Novel Mutations of the PCSK9 Gene Cause Variable Phenotype of Autosomal Dominant Hypercholesterolemia;Allard;Hum. Mutat.,2005
4. NARC-1/PCSK9 and its natural mutants: zymogen cleavage and effects on the low-density lipoprotein (LDL) receptor and LDL cholesterol;Benjannet;J. Biol. Chem.,2004
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