Connection

FABRIZIA FAUSTINELLA to Hyperlipoproteinemia Type I

This is a "connection" page, showing publications FABRIZIA FAUSTINELLA has written about Hyperlipoproteinemia Type I.
  1. Catalytic triad residue mutation (Asp156----Gly) causing familial lipoprotein lipase deficiency. Co-inheritance with a nonsense mutation (Ser447----Ter) in a Turkish family. J Biol Chem. 1991 Aug 05; 266(22):14418-24.
    View in: PubMed
    Score: 0.096
  2. A missense mutation (Trp86----Arg) in exon 3 of the lipoprotein lipase gene: a cause of familial chylomicronemia. Am J Hum Genet. 1992 Jun; 50(6):1275-80.
    View in: PubMed
    Score: 0.025
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.