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Connection

Kenneth Alexander to Polymorphism, Single Nucleotide

This is a "connection" page, showing publications Kenneth Alexander has written about Polymorphism, Single Nucleotide.
  1. Electroretinographic findings in a patient with congenital stationary night blindness due to a novel NYX mutation. Ophthalmic Genet. 2013 Sep; 34(3):167-73.
    View in: PubMed
    Score: 0.059
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.