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Most primary severe hypertriglyceridemias (HTGs) are diagnosed in adults, but their molecular foundations have not been completely elucidated.We aimed to identify rare dysfunctional mutations in genes encoding regulators of lipoprotein lipase (LPL) function in patients with familial and non-familial primary HTG.We sequenced promoters, exons, and exon–intron boundaries of LPL, APOA5, LMF1, and GPIHBP1...
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