Connection

Kenton Holden to Brain Diseases, Metabolic, Inborn

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This is a "connection" page, showing publications Kenton Holden has written about Brain Diseases, Metabolic, Inborn.
Kenton Holden
Connection Strength
0.300
Brain Diseases, Metabolic, Inborn
  1. Persistent growth failure in Prader-Willi syndrome associated with short-chain acyl-CoA dehydrogenase gene variant. J Child Neurol. 2008 Jan; 23(1):112-7.
    View in: PubMed
    Score: 0.300
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.