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A new type of hyperlysinaemia due to a transport defect of lysine into mitochondria

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Journal of Inherited Metabolic Disease

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References

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Authors and Affiliations

  1. Department of Paediatrics, Sapporo Medical College, Sapporo, Japan

    K. Oyanagi, T. Aoyama, A. Tsuchiyama & T. Nakao

  2. Department of Paediatrics, Otaru National Hospital, Otaru, Japan

    N. Uetsuji, K. Wagatsuma & S. Tsugawa

Authors
  1. K. Oyanagi
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  2. T. Aoyama
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  3. A. Tsuchiyama
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  4. T. Nakao
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  5. N. Uetsuji
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  6. K. Wagatsuma
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  7. S. Tsugawa
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Oyanagi, K., Aoyama, T., Tsuchiyama, A. et al. A new type of hyperlysinaemia due to a transport defect of lysine into mitochondria. J Inherit Metab Dis 9, 313–316 (1986). https://doi.org/10.1007/BF01799673

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  • DOI: https://doi.org/10.1007/BF01799673

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