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1. A novel APOA5 splicing mutation IVS2+1g>a in a Japanese chylomicronemia patient.

Author

Okubo M, Ishihara M, Iwasaki T, Ebara T, Aoyama Y, Murase T, and Hattori H

Subjects
Apolipoprotein A-V, Apolipoproteins A blood, DNA Mutational Analysis, Heterozygote, Humans, Hyperlipoproteinemia Type I blood, Hyperlipoproteinemia Type I drug therapy, Hyperlipoproteinemia Type I ethnology, Introns, Japan, Male, Middle Aged, Apolipoproteins A genetics, Asian People genetics, Hyperlipoproteinemia Type I genetics, Mutation, RNA Splice Sites
Published
2009
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