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Severe xanthomatosis associated with familial apolipoprotein E deficiency.
AIM: To present the clinical, dermatological, and histological features of a patient with generalised xanthomatosis, familial apolipoprotein (apo) E deficiency, and unusual type III hyperlipoproteinaemia (HLP). METHODS: The underlying molecular defect was disclosed using molecular biological techniq...
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
1996
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| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC499646/ https://ncbi.nlm.nih.gov/pubmed/9038735 |
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