Apolipoprotein AI mutation Arg-60 causes autosomal dominant amyloidosis.

A mutation in the gene for apolipoprotein AI (apoAI) was identified in an English family with autosomal dominant non-neuropathic systemic amyloidosis. The plasma of all affected individuals contained a variant apoAI with one additional charge, as well as normal apoAI. The propositus was heterozygous...

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Hlavní autoři: Soutar, A K, Hawkins, P N, Vigushin, D M, Tennent, G A, Booth, S E, Hutton, T, Nguyen, O, Totty, N F, Feest, T G, Hsuan, J J
Médium: Artigo
Jazyk:Inglês
Vydáno: 1992
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Research Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC49715/
https://ncbi.nlm.nih.gov/pubmed/1502149
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