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Atypical familial dysbetalipoproteinemia associated with apolipoprotein phenotype E3/3.

Familial dysbetalipoproteinemia has been reported to be associated uniquely with an apolipoprotein E phenotype (E2/2) that occurs in approximately 1% of all persons. We have observed the typical clinical and biochemical characteristics of this disorder in five members of a family, in all of whom the...

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Hlavní autoři: Havel, R J, Kotite, L, Kane, J P, Tun, P, Bersot, T
Médium: Artigo
Jazyk:Inglês
Vydáno: 1983
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1129193/
https://ncbi.nlm.nih.gov/pubmed/6860421
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