Associated Papers
Role of DNA copy number variation in dyslipidemias.
Iacocca MA et al.
Current Opinion in Lipidology, 2018
Mutation analysis of WNT10B in obese children, adolescents and adults.
Van Camp JK et al.
Endocrine, 2013
Multiplex ligation-dependent probe amplification of LDLR enhances molecular diagnosis of familial hypercholesterolemia.
Wang J et al.
Journal of Lipid Research, 2005
Analysis of LDL receptor gene mutations in Italian patients with homozygous familial hypercholesterolemia.
Bertolini S et al.
Arteriosclerosis, Thrombosis, and Vascular Biology, 1999
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