Exclusion of linkage between the human apolipoprotein B gene and abetalipoproteinemia.

Abetalipoproteinemia (ABLP) is a rare autosomal recessive disease characterized by a lack of plasma apolipoprotein B (apo B). In this report, the hypothesis that ABLP is due to rare mutations in the apo B gene was tested. A total of eight ABLP families were studied. Apo B gene RFLPs were used to est...

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Autori principali: Huang, L S, Jänne, P A, de Graaf, J, Cooper, M, Deckelbaum, R J, Kayden, H, Breslow, J L, Decklebaum, R J
Natura: Artigo
Lingua:Inglês
Pubblicazione: 1990
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Research Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC1683822/
https://ncbi.nlm.nih.gov/pubmed/2339706
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