Mutations in LPL, APOC2, APOA5, GPIHBP1 and LMF1 in patients with severe hypertriglyceridaemia

作者: R. P. Surendran , M. E. Visser , S. Heemelaar , J. Wang , J. Peter

DOI: 10.1111/J.1365-2796.2012.02516.X

关键词:

摘要: … In vitro validation revealed that the mutations in LMF1 were not associated with compromised LPL function. Consistent with this, five of the eight LMF1 variants were also found in …

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