The Genetic Spectrum of Familial Hypertriglyceridemia in Oman
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DOI: 10.3389/fgene.2022.886182
Abstract: Familial hypertriglyceridemia (F-HTG) is an autosomal disorder that causes severe elevation of serum triglyceride levels. It is caused by genetic alterations in LPL, APOC2, APOA5, LMF1, and GPIHBP1 genes. The mutation spectrum of F-HTG in… read more here.
Keywords: genetic spectrum; gene; familial hypertriglyceridemia; mutation ... See more keywords