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Molecular basis of familial hypercholesterolemia: An Indian experience
Familial hypercholesterolemia (FH) is an autosomal dominant disease caused by a multitude of low-density lipoprotein (LDL) receptor gene mutations. The LDL receptor is a cell surface trans-membrane protein that mediates the uptake & lysosomal degradation of plasma LDI., thereby providing cholest...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer India
2000
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3454073/ https://ncbi.nlm.nih.gov/pubmed/23105264 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/BF02867540 |
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