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Connection

Robert Hufnagel to Frameshift Mutation

This is a "connection" page, showing publications Robert Hufnagel has written about Frameshift Mutation.
Connection Strength

0.845
  1. Novel TMEM98, MFRP, PRSS56 variants in a large United States high hyperopia and nanophthalmos cohort. Sci Rep. 2020 11 17; 10(1):19986.
    View in: PubMed
    Score: 0.751
  2. De novo frameshift mutation in YAP1 associated with bilateral uveal coloboma and microphthalmia. Ophthalmic Genet. 2022 08; 43(4):513-517.
    View in: PubMed
    Score: 0.052
  3. Variants in myelin regulatory factor (MYRF) cause autosomal dominant and syndromic nanophthalmos in humans and retinal degeneration in mice. PLoS Genet. 2019 05; 15(5):e1008130.
    View in: PubMed
    Score: 0.042

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