Connection

Kenton Holden to Fragile X Mental Retardation Protein

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This is a "connection" page, showing publications Kenton Holden has written about Fragile X Mental Retardation Protein.
Kenton Holden
Connection Strength
0.097
Fragile X Mental Retardation Protein
  1. Severe Hunter syndrome (mucopolysaccharidosis II) phenotype secondary to large deletion in the X chromosome encompassing IDS, FMR1, and AFF2 (FMR2). J Child Neurol. 2012 Jun; 27(6):786-90.
    View in: PubMed
    Score: 0.097
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.