Connection

Kenton Holden to Mutation, Missense

This is a "connection" page, showing publications Kenton Holden has written about Mutation, Missense.
Connection Strength

0.273
  1. Mucolipidosis type IV: a subtle pediatric neurodegenerative disorder. Pediatr Neurol. 2010 Mar; 42(3):223-6.
    View in: PubMed
    Score: 0.082
  2. Expanding the neurologic phenotype of oculodentodigital dysplasia in a 4-generation Hispanic family. J Child Neurol. 2008 Aug; 23(8):901-5.
    View in: PubMed
    Score: 0.073
  3. A novel mutation in the connexin 46 gene (GJA3) causes autosomal dominant zonular pulverulent cataract in a Hispanic family. Mol Vis. 2006 Jul 20; 12:791-5.
    View in: PubMed
    Score: 0.063
  4. POMGnT1 gene alterations in a family with neurological abnormalities. Ann Neurol. 2004 Jul; 56(1):143-8.
    View in: PubMed
    Score: 0.055
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.