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Autosomal recessive spino-cerebellar ataxia type 10 (SCAR10): clinical presentation associated with c.289delA ANO10 gene variant

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Data availability

The data that support the findings of this study are available on request from the corresponding author, DN.

References

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Authors and Affiliations

  1. Department of Medicine and Surgery, Unit of Neurology, Neurophysiology, Neurobiology and Psychiatry, Università Campus Bio-Medico Di Roma, Via Alvaro del Portillo, 21 - 00128, Rome, Italy

    Davide Norata

  2. Neurological Clinic and Stroke Unit, Department of Experimental and Clinical Medicine (DiMSC), Marche Polytechnic University, Via Conca 71, 60020, Ancona, Italy

    Davide Norata

  3. Unit of Neurophysiopathology, Department of Biomedicine, Neuroscience and Advanced Diagnostic (BIND), University of Palermo, 90129, Palermo, Italy

    Paolo Alonge, Antonino Lupica, Vanessa Costa, Filippo Brighina & Vincenzo Di Stefano

  4. Oasi Research Institute-IRCCS, 94018, Troina, Italy

    Lucia Grillo, Francesco Calì & Maurizio Sturnio

Authors
  1. Davide Norata
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  2. Paolo Alonge
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  3. Lucia Grillo
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  4. Francesco Calì
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  5. Maurizio Sturnio
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  6. Antonino Lupica
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  7. Vanessa Costa
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  8. Filippo Brighina
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  9. Vincenzo Di Stefano
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Corresponding author

Correspondence to Davide Norata.

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The study was performed in accordance with the ethical standards as laid down in the 1964 Declaration of Helsinki and its later amendments or comparable ethical standards. The participant has consented to the submission of the case report to the journal.

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The authors declare no competing interests.

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Norata, D., Alonge, P., Grillo, L. et al. Autosomal recessive spino-cerebellar ataxia type 10 (SCAR10): clinical presentation associated with c.289delA ANO10 gene variant. Neurol Sci 45, 1283–1286 (2024). https://doi.org/10.1007/s10072-023-07104-0

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  • DOI: https://doi.org/10.1007/s10072-023-07104-0

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