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Spastizin mutation in hereditary spastic paraplegia with thin corpus callosum

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Acknowledgments

We thank the patient and the parents for participating in this study. We thankfully acknowledge DST-FIST, Government of India, Manipal University and TIFAC Core for the infrastructure support.

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Authors and Affiliations

  1. Department of Cell and Molecular Biology, School of Life Sciences, Manipal University, Manipal, Karnataka, 576104, India

    Sanjiban Chakrabarty & Kapaettu Satyamoorthy

  2. Department of Neurology, Kasturba Medical College, Manipal University, Manipal, Karnataka, 576104, India

    Nimish Vijayakumar & Kurupath Radhakrishnan

Authors
  1. Sanjiban Chakrabarty
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  2. Nimish Vijayakumar
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  3. Kurupath Radhakrishnan
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  4. Kapaettu Satyamoorthy
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Corresponding author

Correspondence to Kapaettu Satyamoorthy.

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The authors declare no conflict of interest.

Ethical standard

This study followed ethical standards in conducting all diagnostic procedures. The patient was informed about the intention to publish the cases report and gave their written consent.

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Chakrabarty, S., Vijayakumar, N., Radhakrishnan, K. et al. Spastizin mutation in hereditary spastic paraplegia with thin corpus callosum. J Neurol 263, 2130–2132 (2016). https://doi.org/10.1007/s00415-016-8258-1

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  • DOI: https://doi.org/10.1007/s00415-016-8258-1

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