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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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Dettagli Bibliografici
Autore principale: Feussner, G
Natura: Artigo
Lingua:Inglês
Pubblicazione: 1996
Soggetti:
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC499646/
https://ncbi.nlm.nih.gov/pubmed/9038735
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