Heterozygous ATP-binding Cassette Transporter G5 Gene Deficiency and Risk of Coronary Artery Disease

BACKGROUND: 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) variants – in the ATP-binding cassette transporter...

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Опубликовано в: :Circ Genom Precis Med
Главные авторы: Nomura, Akihiro, Emdin, Connor A., Won, Hong Hee, Peloso, Gina M., Natarajan, Pradeep, Ardissino, Diego, Danesh, John, Schunkert, Heribert, Correa, Adolfo, Bown, Matthew J., Samani, Nilesh J., Erdmann, Jeanette, McPherson, Ruth, Watkins, Hugh, Saleheen, Danish, Elosua, Roberto, Kawashiri, Masa-aki, Tada, Hayato, Gupta, Namrata, Shah, Svati H., Rader, Daniel J., Gabriel, Stacey, Khera, Amit V., Kathiresan, Sekar
Формат: Artigo
Язык:Inglês
Опубликовано: 2020
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Article
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC7983048/
https://ncbi.nlm.nih.gov/pubmed/32862661
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1161/CIRCGEN.119.002871
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