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Lpld Is A Rare Autosomal Recessive Disorder, Characterized By The Presence Of Marked Chylomicronemia And Hence Hypertriglyceridemia.

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We Studied The Influence Of Polymorphisms In Lipoprotein Lipase Lpl Gene, Betafibrinogen Gene Fibb And Environmental Factors On Plasma Fibrinogen Levels In.

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