Abstract 18715: Clinical Characteristics of Double Heterozygotes With PCSK9 Gain-of-Function Mutations and LDLR Mutations

Atsushi Nohara(Kanazawa University), Hiroshi Mabuchi(Kanazawa University), Takeshi Kobayashi(Nihon Institute of Medical Science), Chiaki Nakanishi(Kanazawa University), Masa‐aki Kawashiri(Kanazawa University), Mika Mori(Kanazawa University), Masakazu Yamagishi, Hayato Tada(Kanazawa University), Akihiro Inazu(Kanazawa University), Mie Yoshida(Kanazawa University), Kunimasa Yagi(University of Ulsan)
Circulation
November 11, 2016
Cited by 0

Related Papers

Increased High-Density Lipoprotein Levels Caused by a Common Cholesteryl-Ester Transfer Protein Gene Mutation
|New England Journal of Medicine|1990|865
Molecular basis of lipid transfer protein deficiency in a family with increased high-density lipoproteins
|Nature|1989|465
T wave peak-to-end interval and QT dispersion in acquired long QT syndrome: a new index for arrhythmogenicity
|Clinical Science|2003|313
T‐peak to T‐end interval may be a better predictor of high‐risk patients with hypertrophic cardiomyopathy associated with a cardiac troponin i mutation than qt dispersion
|Clinical Cardiology|2002|267
Intermediate-density lipoprotein and cholesterol-rich very low density lipoprotein in angiographically determined coronary artery disease.
|Circulation|1981|250