A rare STAP1 mutation incompletely associated with familial hypercholesterolemia

Published 2018 View Full Article

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Title
A rare STAP1 mutation incompletely associated with familial hypercholesterolemia
Authors
Keywords
Autosomal dominant hypercholesterolemia, Phenotype-genotype correlation, Molecular diagnosis, LDLR, APOB
Journal
CLINICA CHIMICA ACTA
Volume 487, Issue -, Pages 270-274
Publisher
Elsevier BV
Online
2018-10-09
DOI
10.1016/j.cca.2018.10.014

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