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Effect of the amyloidogenic L75P apolipoprotein A-I variant on HDL subpopulations
BACKGROUND: Hereditary amyloidosis due to mutations of apolipoprotein A-I (apoA-I) is a rare disease characterized by the deposition of amyloid fibrils constituted by the N-terminal fragment of apoA-I in several organs. L75P is a variant of apoA-I associated with systemic amyloidosis predominantly i...
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| Huvudupphovsmän: | , , , , , , , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
Elsevier
2011
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3096778/ https://ncbi.nlm.nih.gov/pubmed/21458433 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.cca.2011.03.027 |
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