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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Publicado no:Circ Genom Precis Med
Main Authors: 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
Formato: Artigo
Idioma:Inglês
Publicado em: 2020
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Article
Acesso em linha: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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