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Homozygous familial hypercholesterolemia mutant with a defect in internalization of low density lipoprotein.
During studies on binding of low density lipoprotein (LDL) to fibroblasts from patients with the homozygous form of familial hypercholesterolemia (FH), a unique line was derived from subject M.N. This line could bind as much LDL as normal cells, or even more. However, like fibroblasts from other pat...
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| Publicat a: | Proc Natl Acad Sci U S A |
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| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
National Academy of Sciences
1981
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC320351/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/6272292/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.78.8.5151 |
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