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Photoreceptors in evolution and disease

Nature Genetics volume 40, pages 1275–1276 (2008)Cite this article

A new study identifies the gene that, when mutated, causes autosomal recessive retinitis pigmentosa 25 (arRP25). The RP25 gene encodes an ortholog of Drosophila spacemaker (eyes shut), thus emphasizing common biological functions between Drosophila sensory systems and the human eye.

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Figure 1: A comparison of Drosophila and human retinas.

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Authors and Affiliations

  1. Boaz Cook is in the Department of Cell Biology, The Scripps Research Institute, La Jolla, California 92037, USA. bcook@scripps.edu,

    Boaz Cook

  2. Andrew C. Zelhof is in the Department of Biology, Indiana University, Bloomington, Indiana 47405, USA. azelhof@indiana.edu,

    Andrew C Zelhof

Authors
  1. Boaz Cook
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  2. Andrew C Zelhof
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Cook, B., Zelhof, A. Photoreceptors in evolution and disease. Nat Genet 40, 1275–1276 (2008). https://doi.org/10.1038/ng1108-1275

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