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Connection

Robert Hufnagel to Optic Atrophy, Autosomal Dominant

This is a "connection" page, showing publications Robert Hufnagel has written about Optic Atrophy, Autosomal Dominant.
  1. Antisense Oligonucleotide STK-002 Increases OPA1 in Retina and Improves Mitochondrial Function in Autosomal Dominant Optic Atrophy Cells. Nucleic Acid Ther. 2024 10; 34(5):221-233.
    View in: PubMed
    Score: 0.245
  2. 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: 0.130

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