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De novo mutations in the CRX homeobox gene associated with Leber congenital amaurosis

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Authors and Affiliations

  1. Program in Developmental Biology, The Research Institute, Hospital for Sick Children, Toronto, Ontario, Canada, M5G1X8

    Carol L. Freund, Brenda L. Muskat & Roderick R. Mclnnes

  2. Department of Ophthalmology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA

    Qing-Ling Wang, Shiming Chen & Donald J. Zack

  3. Departments of Molecular Biology and Genetics and Neuroscience, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA

    Donald J. Zack

  4. Department of Opthalmology, University of Iowa Medical School, 200 Hawkins Drive, Iowa City, Iowa, 52242, USA

    Carmella D. Wiles & Edwin M. Stone

  5. Department of Pediatrics and Howard Hughes Medical Institute, University of Iowa, Iowa City, Iowa, USA

    Val C. Sheffield

  6. Scheie Eye Institute, University of Pennsylvania, Philadelphia, Pennsylvania, USA

    Samuel G. Jacobson

Authors
  1. Carol L. Freund
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  2. Qing-Ling Wang
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  3. Shiming Chen
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  4. Brenda L. Muskat
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  5. Carmella D. Wiles
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  6. Val C. Sheffield
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  7. Samuel G. Jacobson
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  8. Roderick R. Mclnnes
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  9. Donald J. Zack
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  10. Edwin M. Stone
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Freund, C., Wang, QL., Chen, S. et al. De novo mutations in the CRX homeobox gene associated with Leber congenital amaurosis. Nat Genet 18, 311–312 (1998). https://doi.org/10.1038/ng0498-311

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