부가기능
NOVEL COMPOUND HETEROZYGOUS MUTATIONS FOR LIPOPROTEIN LIPASE DEFICIENCY: A G-TO-T TRANSVERSION AT THE FIRST POSITION OF EXON 5 CAUSING G154V MISSENSE MUTATION AND A 5' SPLICE SITE MUTATION OF INTRON 8 LPL gene mutation . hypertriglyceridemia . first nucleotide . first base . acceptor splice site . donor splice site . cryptic splice site/
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