The Genetic Basis of Hypertriglyceridemia
نویسندگان
چکیده
منابع مشابه
The molecular basis of severe hypertriglyceridemia: from genetic counseling to gene therapy.
C-II (Apo cII), lipase maturation factor 1 (LFM1), glycosylphosphatidylinositolanchored high density lipoprotein binding protein 1 (GPIHBP1) and apoprotein A5 (APO5) [7]. The accurate diagnosis of the genetic cause in a specific family is now feasible and enables detection of novel mutations in candidate genes, as shown by Behar et al. in their current report [6]. Another group is Israel used a...
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Hyperuricemia and hypertriglyceridemia: metabolic basis for the association.
Hypertriglyceridemia has been reported frequently in patients with hyperuricemia and gout. The current studies have evaluated this relationship. To examine whether hypertriglyceridemia leads to hyperuricemia, IV intralipid was given to three gouty patients. Triglycerides increased from 169 to 700 mg/dl for three hours but caused no change in serum urate level or urine uric acid and oxypurine ex...
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ژورنال
عنوان ژورنال: Current Atherosclerosis Reports
سال: 2021
ISSN: 1523-3804,1534-6242
DOI: 10.1007/s11883-021-00939-y