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Connection

Kenneth Alexander to Eye Diseases, Hereditary

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This is a "connection" page, showing publications Kenneth Alexander has written about Eye Diseases, Hereditary.
Kenneth Alexander
Connection Strength
0.109
Eye Diseases, Hereditary
  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: 0.109
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.