Connection

Loreto Gesualdo to Mutation

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This is a "connection" page, showing publications Loreto Gesualdo has written about Mutation.
Loreto Gesualdo
Connection Strength
0.233
Mutation
  1. Further phenotypic heterogeneity of CoQ10 deficiency associated with steroid resistant nephrotic syndrome and novel COQ2 and COQ6 variants. Clin Genet. 2017 08; 92(2):224-226.
    View in: PubMed
    Score: 0.158
  2. Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations. Am J Hum Genet. 2017 Nov 02; 101(5):789-802.
    View in: PubMed
    Score: 0.041
  3. Novel INF2 mutations in an Italian cohort of patients with focal segmental glomerulosclerosis, renal failure and Charcot-Marie-Tooth neuropathy. Nephrol Dial Transplant. 2014 Sep; 29 Suppl 4:iv80-6.
    View in: PubMed
    Score: 0.033
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.