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

doi:10.1111/epi.12317

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 journal › Article

Original language	English
Pages (from-to)	1333
Number of pages	1
Journal	Epilepsia
Volume	54
Issue number	7
DOIs	https://doi.org/10.1111/epi.12317
Publication status	Published - Jul 2013

ASJC Scopus subject areas

Clinical Neurology
Neurology

Access to Document

10.1111/epi.12317

Cite this

Canafoglia, L., Gennaro, E., Capovilla, G., Gobbi, G., Boni, A., Beccaria, F., Viri, M., Michelucci, R., Agazzi, P., Assereto, S., Coviello, D. A., Di Stefano, M., Rossi Sebastiano, D., Franceschetti, S., & Zara, F. (2013). 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)). Epilepsia, 54(7), 1333. https://doi.org/10.1111/epi.12317

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

In: Epilepsia, Vol. 54, No. 7, 07.2013, p. 1333.

Research output: Contribution to journal › Article

Canafoglia, L, Gennaro, E, Capovilla, G, Gobbi, G, Boni, A, Beccaria, F, Viri, M, Michelucci, R, Agazzi, P, Assereto, S, Coviello, DA, Di Stefano, M, Rossi Sebastiano, D , Franceschetti, S & Zara, F 2013, '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))', Epilepsia, vol. 54, no. 7, pp. 1333. https://doi.org/10.1111/epi.12317

Canafoglia, L. ; Gennaro, E. ; Capovilla, G. ; Gobbi, G. ; Boni, A. ; Beccaria, F. ; Viri, M. ; Michelucci, R. ; Agazzi, P. ; Assereto, S. ; Coviello, D. A. ; Di Stefano, M. ; Rossi Sebastiano, D. ; Franceschetti, S. ; Zara, F. / 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)). In: Epilepsia. 2013 ; Vol. 54, No. 7. pp. 1333.

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