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Reply to: Diagnosing MELAS requires not only an mtDNA variant but also an appropriate phenotype

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The Original Article was published on 28 March 2019

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Authors and Affiliations

  1. Department of Ophthalmology, Gifu University Graduate School of Medicine, 1-1 Yanagido, Gifu-shi, 501-1194, Japan

    Kenji Ozawa, Kiyofumi Mochizuki & Yusuke Manabe

  2. Department of Neurology and Geriatrics, Gifu University Graduate School of Medicine, 1-1 Yanagido, Gifu-shi, 501-1194, Japan

    Nobuaki Yoshikura & Takayoshi Shimohata

  3. Department of Neuromuscular Research, National Institute of Neurology and Psychiatry, National Center of Neurology and Psychiatry, Tokyo, Japan

    Ichizo Nishino

  4. Mental Retardation and Birth Defect Research, National Institute of Neurology and Psychiatry, National Center of Neurology and Psychiatry, Tokyo, Japan

    Yu-ichi Goto

  5. Medical Genome Center, National Center of Neurology and Psychiatry, Tokyo, Japan

    Yu-ichi Goto

Authors
  1. Kenji Ozawa
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  2. Kiyofumi Mochizuki
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  3. Yusuke Manabe
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  4. Nobuaki Yoshikura
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  5. Takayoshi Shimohata
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  6. Ichizo Nishino
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  7. Yu-ichi Goto
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Corresponding author

Correspondence to Kenji Ozawa.

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Ozawa, K., Mochizuki, K., Manabe, Y. et al. Reply to: Diagnosing MELAS requires not only an mtDNA variant but also an appropriate phenotype. Doc Ophthalmol 138, 257–258 (2019). https://doi.org/10.1007/s10633-019-09688-5

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  • DOI: https://doi.org/10.1007/s10633-019-09688-5

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