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Mice lacking global Stap1 expression do not manifest hypercholesterolemia
BACKGROUND: Autosomal dominant familial hypercholesterolemia (ADH; MIM#143890) is one of the most common monogenic disorders characterized by elevated circulatory LDL cholesterol. Initial studies in humans with ADH identified a potential relationship with variants of the gene encoding signal transdu...
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| Publicado en: | BMC Med Genet |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
BioMed Central
2020
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7685646/ https://ncbi.nlm.nih.gov/pubmed/33228548 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-020-01176-x |
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