A new SCARB2 mutation in a patient with progressive myoclonus ataxia without renal failure

Authors

  • Claudia Perandones MD, MSC, PhD,

    1. Parkinson's Disease and Movement Disorders Program, Hospital de Clínicas José de San Martín, University of Buenos Aires, Argentina
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  • Luis Alejandro Pellene PhD,

    1. Parkinson's Disease and Movement Disorders Program, Hospital de Clínicas José de San Martín, University of Buenos Aires, Argentina
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  • Federcio Micheli MD, PhD

    Corresponding author
    1. National Administration of Laboratories and Health Institutes of Argentina, Argentina
    • Correspondence to: Federico Micheli MD, PhD, Parkinson's Disease and Movement Disorder Program, Mailing address: Juncal 1695 Piso 5 “J” zip code 1062, Buenos Aires, Argentina, Email: fmicheli@fibertel.com.ar

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  • Funding agencies: None.

  • Relevant conflicts of interest/financial disclosures: Nothing to report.

No abstract is available for this article.

Ancillary