Connection

Kenton Holden to Amino Acid Substitution

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This is a "connection" page, showing publications Kenton Holden has written about Amino Acid Substitution.
Kenton Holden
Connection Strength
0.033
Amino Acid Substitution
  1. A novel familial autosomal dominant mutation in ARID1B causing neurodevelopmental delays, short stature, and dysmorphic features. Am J Med Genet A. 2016 12; 170(12):3313-3318.
    View in: PubMed
    Score: 0.033
Connection Strength

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Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.