Connection

GRAEME MARDON to Nicotinamide-Nucleotide Adenylyltransferase

This is a "connection" page, showing publications GRAEME MARDON has written about Nicotinamide-Nucleotide Adenylyltransferase.
  1. NMNAT1 E257K variant, associated with Leber Congenital Amaurosis (LCA9), causes a mild retinal degeneration phenotype. Exp Eye Res. 2018 08; 173:32-43.
    View in: PubMed
    Score: 0.156
  2. Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degeneration. Nat Genet. 2012 Sep; 44(9):1035-9.
    View in: PubMed
    Score: 0.105
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.