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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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Circ Genom Precis Med
Prif Awduron: 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
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: 2020
Pynciau:
Article
Mynediad Ar-lein: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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