Reporting a new mutation at the SLC20A2 gene in a Brazilian family with idiopathic basal ganglia calcification – Correction

Authors

  • R. R. de Lemos,

    1. Fundación Pública Galega de Medicina Xenómica-SERGAS-IDIS (Hospital Clínico Universitario), Universidad de Santiago de Compostela, Santiago de Compostela, Spain
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  • J. B. M. M. Ferreira,

    1. Keizo Asami Laboratory, Universidade Federal de Pernambuco, Recife-PE
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  • J. R. M. de Oliveira

    Corresponding author
    1. Keizo Asami Laboratory, Universidade Federal de Pernambuco, Recife-PE
    2. Neuropsychiatry department, Universidade Federal de Pernambuco, Recife-PE, Brazil
    • Correspondence: J. R. M. Oliveira, Department of Neuropsychiatry, Universidade Federal de Pernambuco (UFPE), Av. Prof. Moraes Rego, 1235. Cidade Universitária, Recife – PE, Brazil (tel.: +55 81 8781 9856; fax: +55 81 2126 8485; e-mail: joao.ricardo@ufpe.br).

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No abstract is available for this article.

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