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Connection

Louis Philipson to Point Mutation

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This is a "connection" page, showing publications Louis Philipson has written about Point Mutation.
Louis Philipson
Connection Strength
0.106
Point Mutation
  1. Microcephaly, epilepsy, and neonatal diabetes due to compound heterozygous mutations in IER3IP1: insights into the natural history of a rare disorder. Pediatr Diabetes. 2014 May; 15(3):252-6.
    View in: PubMed
    Score: 0.106
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.