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Identification and Molecular Characterization of New PCSK9 Missense Mutations Associated with Familial Hypecholesterolemia (FH)

✍ Scribed by Vivienne M. Homer; Francesca Charlton; Andrew D. Laurie; David A. Marais; Nicola J. Hurndell; David R. Sullivan; Philip J. Barter; Kerry-Ann Rye; Peter M. George; Gilles C. Lambert

Book ID: 119254755
Publisher: Elsevier Science
Year: 2007
Tongue: English
Weight: 90 KB
Volume: 16
Category: Article
ISSN: 1443-9506
DOI: 10.1016/j.hlc.2007.06.219

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