Tangier Disease
Tangier disease is a rare familial disorder characterized by enlarged orange tonsils, transient peripheral neuropathy, hepatosplenomegaly, and lymphadenopathy, as well as striking reductions in plasma high density lipoproteins (HDL) and their major protein constituents, apolipoproteins (apo)A-I and...
Uloženo v:
| Vydáno v: | J Clin Invest |
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| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
American Society for Clinical Investigation
1982
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC370306/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/7130397/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI110705 |
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