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gpihbp1 protein, human
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Marked hypertriglyceridemia with a novel splicing mutation in GPIHBP1.
Circulating GPIHBP1 levels and microvascular complications in patients with type 2 diabetes: A cross…
Familial chylomicronemia syndrome: case reports of siblings with deletions of the GPIHBP1 gene.
Development of hypertriglyceridemia due to GPIHBP1 autoantibodies prior to clinical diagnosis of sys…
Chylomicronemia from GPIHBP1 autoantibodies.
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A 12-Week Study to Assess the Efficacy Safety and Tolerability of Gemcabene in Subjects With Severe …
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