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A novel mutation in ATP13A2 gene in a patient with complicated hereditary spastic paraplegia accompanied by tubulopathy

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References

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Authors and Affiliations

  1. Department of Neurology, Hacettepe University Faculty of Medicine, 06100, Sıhhıye, Ankara, Turkey

    Berin Inan, Filiz Azman & Serap Saygi

  2. Damagen Genetic Diagnostic Center, Ankara, Turkey

    Dilek Aktas

  3. Division of Pediatric Metabolism, Department of Pediatrics, Hacettepe University Faculty of Medicine, Ankara, Turkey

    Yilmaz Yildiz

Authors
  1. Berin Inan
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  2. Filiz Azman
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  3. Dilek Aktas
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  4. Yilmaz Yildiz
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  5. Serap Saygi
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Correspondence to Berin Inan.

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Genetic analysis was performed for clinical diagnosis only, so approval of ethics committee was not required.

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Inan, B., Azman, F., Aktas, D. et al. A novel mutation in ATP13A2 gene in a patient with complicated hereditary spastic paraplegia accompanied by tubulopathy. Acta Neurol Belg 123, 1985–1987 (2023). https://doi.org/10.1007/s13760-022-02021-z

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  • DOI: https://doi.org/10.1007/s13760-022-02021-z

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