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Connection

Robert Hufnagel to Membrane Proteins

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

1.808
  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: 0.731
  2. The peroxisomal disorder spectrum and Heimler syndrome: Deep phenotyping and review of the literature. Am J Med Genet C Semin Med Genet. 2020 09; 184(3):618-630.
    View in: PubMed
    Score: 0.721
  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: 0.164
  4. Using human sequencing to guide craniofacial research. Genesis. 2019 01; 57(1):e23259.
    View in: PubMed
    Score: 0.160
  5. Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder. Nat Genet. 2015 Aug; 47(8):926-32.
    View in: PubMed
    Score: 0.032

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