Erratum: Electroclinical presentation and genotype-phenotype relationships in patients with Unverricht-Lundborg disease carrying compound heterozygous CSTB point and indel mutations (Epilepsia (2012) 53 (2120-2127))

L. Canafoglia, E. Gennaro, G. Capovilla, G. Gobbi, A. Boni, F. Beccaria, M. Viri, R. Michelucci, P. Agazzi, S. Assereto, D. A. Coviello, M. Di Stefano, D. Rossi Sebastiano, S. Franceschetti, F. Zara

Research output: Contribution to journalArticlepeer-review

Original languageEnglish
Pages (from-to)1333
Number of pages1
Issue number7
Publication statusPublished - Jul 2013

ASJC Scopus subject areas

  • Clinical Neurology
  • Neurology

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