A complex phenotype in a child with familial HDL deficiency due to a novel frameshift mutation in APOA1 gene (apoA-I Guastalla )

Published 2015 View Full Article

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Title
A complex phenotype in a child with familial HDL deficiency due to a novel frameshift mutation in APOA1 gene (apoA-I Guastalla )
Authors
Keywords
APOA1, mutation, Truncated apoA-I, Hypertriglyceridemia, Metabolic syndrome, β-thalassemia trait
Journal
Journal of Clinical Lipidology
Volume 9, Issue 6, Pages 837-846
Publisher
Elsevier BV
Online
2015-09-19
DOI
10.1016/j.jacl.2015.09.001

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