Loading...
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...
Saved in:
| Published in: | Proc Natl Acad Sci U S A |
|---|---|
| Main Authors: | , , , |
| Format: | Artigo |
| Language: | Inglês |
| Published: |
National Academy of Sciences
1981
|
| Subjects: | |
| Online Access: | 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 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|