Connection

Giuseppe Novelli to Pyrroline Carboxylate Reductases

This is a "connection" page, showing publications Giuseppe Novelli has written about Pyrroline Carboxylate Reductases.
  1. De Barsy Syndrome: a genetically heterogeneous autosomal recessive cutis laxa syndrome related to P5CS and PYCR1 dysfunction. Am J Med Genet A. 2012 Apr; 158A(4):927-31.
    View in: PubMed
    Score: 0.125
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.