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

✍ Scribed by André J. Tremblay; Benoı̂t Lamarche; Isabelle Ruel; Jean-Charles Hogue; Jean Bergeron; Claude Gagné; Patrick Couture

• Book ID: 118420214
• Publisher: Elsevier Science
• Year: 2004
• Tongue: English
• Weight: 90 KB
• Volume: 172
• Category: Article
• ISSN: 0021-9150
• DOI: 10.1016/j.atherosclerosis.2003.11.011