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Connection

Ronald Kingsley to Mutation

This is a "connection" page, showing publications Ronald Kingsley has written about Mutation.
Connection Strength

0.356
  1. Expanding the Mutation Spectrum for Inherited Retinal Diseases. Genes (Basel). 2024 Dec 28; 16(1).
    View in: PubMed
    Score: 0.182
  2. Variable expressivity in patients with autosomal recessive retinitis pigmentosa associated with the gene CNGB1. Ophthalmic Genet. 2021 02; 42(1):15-22.
    View in: PubMed
    Score: 0.136
  3. Novel mutation in the TIMP3 gene causes Sorsby fundus dystrophy. Arch Ophthalmol. 2002 Mar; 120(3):376-9.
    View in: PubMed
    Score: 0.037
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.

THIS IS A DEVELOPMENT VERSION OF PROFILES. PLEASE GO TO THE PRODUCTION ENVIRONMENT FOR UPDATES