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Retinitis pigmentosa and mucopolysaccharidosis type II: an extremely attenuated phenotype

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  • Published:
Journal of Inherited Metabolic Disease

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Authors and Affiliations

  1. Department of Pediatrics and Medical Education Development Center, Gifu University Graduate School of Medicine, Yanagido 1-1, Gifu, 501-1194, Japan

    Y. Suzuki & T. Kato

  2. Department of Ophthalmology, Gifu University Graduate School of Medicine, Gifu, Japan

    A. Aoyama

  3. Division of Genomic Research, Life Science Research Center, Gifu University, Gifu, Japan

    N. Shimozawa

  4. Orii Clinic, Gifu, Japan

    T. Orii

Authors
  1. Y. Suzuki
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  2. A. Aoyama
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  3. T. Kato
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  4. N. Shimozawa
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  5. T. Orii
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Corresponding author

Correspondence to Y. Suzuki.

Additional information

Communicating editor: Guy Besley

Competing interests: None declared

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Cite this article

Suzuki, Y., Aoyama, A., Kato, T. et al. Retinitis pigmentosa and mucopolysaccharidosis type II: an extremely attenuated phenotype. J Inherit Metab Dis 32, 582–583 (2009). https://doi.org/10.1007/s10545-009-1204-y

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  • DOI: https://doi.org/10.1007/s10545-009-1204-y

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