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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...
Wedi'i Gadw mewn:
| Cyhoeddwyd yn: | Circ Genom Precis Med |
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| Prif Awduron: | , , , , , , , , , , , , , , , , , , , , , , , |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
2020
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| Pynciau: | |
| 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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