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Genetics of Hypertriglyceridemia
Hypertriglyceridemia, a commonly encountered phenotype in cardiovascular and metabolic clinics, is surprisingly complex. A range of genetic variants, from single-nucleotide variants to large-scale copy number variants, can lead to either the severe or mild-to-moderate forms of the disease. At the ge...
Tallennettuna:
| Julkaisussa: | Front Endocrinol (Lausanne) |
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| Päätekijät: | , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Frontiers Media S.A.
2020
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7393009/ https://ncbi.nlm.nih.gov/pubmed/32793115 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fendo.2020.00455 |
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