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

Authors

  • Rosa Guerrero-López PhD,

    1. Neurology Laboratory-Epilepsy Unit, Neurology Department IIS—Fundación Jiménez Díaz, Madrid, Spain, and Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER) Madrid, Spain
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  • Pedro J. García-Ruiz MD, PhD,

    1. Movements Disorder Unit, Neurology Deparment, Fundación Jiménez Díaz, Madrid, Spain
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  • Beatriz G. Giráldez MD,

    1. Neurology Laboratory-Epilepsy Unit, Neurology Department IIS—Fundación Jiménez Díaz, Madrid, Spain, and Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER) Madrid, Spain
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  • Carmen Durán-Herrera MD,

    1. Neurology Department, Hospital Infanta Cristina, Badajoz, Spain
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  • Maria Rosa Querol-Pascual MD,

    1. Neurology Department, Hospital Infanta Cristina, Badajoz, Spain
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  • José María Ramírez-Moreno MD,

    1. Neurology Department, Hospital Infanta Cristina, Badajoz, Spain
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  • Sebastián Más PhD,

    1. Nephrology Laboratory, IIS—Fundación Jiménez Díaz, Madrid, Spain
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  • José M. Serratosa MD, PhD

    Corresponding author
    1. Neurology Laboratory-Epilepsy Unit, Neurology Department IIS—Fundación Jiménez Díaz, Madrid, Spain, and Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER) Madrid, Spain
    • Neurology Laboratory-Epilepsy Unit, Neurology Department IIS—Fundación Jiménez Díaz, Madrid, Spain, and Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER) Madrid, Spain

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  • Funding agencies: This work was supported by grants from the Spanish Ministry of Education and Science (SAF2007-61003, SAF2010-18586).

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

  • §

    Full financial disclosures and author roles may be found in the online version of this article.

No abstract is available for this article.

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