Lack of evidence for reduced plasma apo B48 catabolism in patients with heterozygous familial hypercholesterolemia carrying the same null LDL receptor gene mutation

Author： Tremblay A.J.   Lamarche B.   Ruel I.   Hogue J.-C.   Bergeron J.   Gagne C.   Couture P.  

Publisher： Elsevier

ISSN： 0021-9150

Source： Atherosclerosis, Vol.172, Iss.2, 2004-02, pp. : 367-373

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