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 › peer-review

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

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10.1111/epi.12317

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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 › peer-review

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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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))

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