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[Some cases of hypertriglyceridaemia in humans are caused by GPIHBP1 mutations that interfere with the ability of GPIHBP1 to bind to LPL, and some are caused by LPL mutations that impair the ability of LPL to bind to GPIHBP1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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