Heterozygous ABCG5 gene deficiency and risk of coronary artery disease

Heterozygous ABCG5 gene deficiency and risk of coronary artery disease

<p><strong>Background:</strong><br /> Familial sitosterolemia is a rare Mendelian disorder characterized by hyperabsorption and decreased biliary excretion of dietary sterols. Affected individuals typically have complete genetic deficiency—homozygous loss-of-function (LoF) va...

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Main Authors: Nomura, A, Emdin, CA, Won, HH, Peloso, GM, Natarajan, P, Ardissino, D, Danesh, J, Schunkert, H, Correa, A, Bown, MJ, Samani, NJ, Erdmann, J, McPherson, R, Watkins, H, Saleheen, D, Elosua, R, Kawashiri, M-A, Tada, H, Gupta, N, Shah, SH, Rader, DJ, Gabriel, S, Khera, AV, Kathiresan, S
Format: Journal article
Language:English
Published: American Heart Association 2020

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