Erratum: A novel pedigree with familial cortical myoclonic tremor and epilepsy (FCMTE): Clinical characterization, refinement of the FCMTE2 locus, and confirmation of a founder haplotype (Epilepsia (2013) 54 (1298-1306))

L. Licchetta; T. Pippucci; F. Bisulli; G. Cantalupo; P. Magini; L. Alvisi; S. Baldassari; P. Martinelli; I. Naldi; N. Vanni; R. Liguori; M. Seri; P. Tinuper

doi:10.1111/epi.12384

Erratum: A novel pedigree with familial cortical myoclonic tremor and epilepsy (FCMTE): Clinical characterization, refinement of the FCMTE2 locus, and confirmation of a founder haplotype (Epilepsia (2013) 54 (1298-1306))

L. Licchetta, T. Pippucci, F. Bisulli, G. Cantalupo, P. Magini, L. Alvisi, S. Baldassari, P. Martinelli, I. Naldi, N. Vanni, R. Liguori, M. Seri, P. Tinuper

Istituto Scienze Neurologiche

Research output: Contribution to journal › Article › peer-review

Original language	English
Pages (from-to)	1709
Number of pages	1
Journal	Epilepsia
Volume	54
Issue number	9
DOIs	https://doi.org/10.1111/epi.12384
Publication status	Published - Sep 2013

ASJC Scopus subject areas

Clinical Neurology
Neurology

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10.1111/epi.12384

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Licchetta, L., Pippucci, T., Bisulli, F., Cantalupo, G., Magini, P., Alvisi, L., Baldassari, S., Martinelli, P., Naldi, I., Vanni, N., Liguori, R., Seri, M., & Tinuper, P. (2013). Erratum: A novel pedigree with familial cortical myoclonic tremor and epilepsy (FCMTE): Clinical characterization, refinement of the FCMTE2 locus, and confirmation of a founder haplotype (Epilepsia (2013) 54 (1298-1306)). Epilepsia, 54(9), 1709. https://doi.org/10.1111/epi.12384

Erratum : A novel pedigree with familial cortical myoclonic tremor and epilepsy (FCMTE): Clinical characterization, refinement of the FCMTE2 locus, and confirmation of a founder haplotype (Epilepsia (2013) 54 (1298-1306)). / Licchetta, L.; Pippucci, T.; Bisulli, F.; Cantalupo, G.; Magini, P.; Alvisi, L.; Baldassari, S.; Martinelli, P.; Naldi, I.; Vanni, N.; Liguori, R.; Seri, M.; Tinuper, P.

In: Epilepsia, Vol. 54, No. 9, 09.2013, p. 1709.

Research output: Contribution to journal › Article › peer-review

Licchetta, L, Pippucci, T, Bisulli, F, Cantalupo, G, Magini, P, Alvisi, L, Baldassari, S, Martinelli, P, Naldi, I, Vanni, N, Liguori, R, Seri, M & Tinuper, P 2013, 'Erratum: A novel pedigree with familial cortical myoclonic tremor and epilepsy (FCMTE): Clinical characterization, refinement of the FCMTE2 locus, and confirmation of a founder haplotype (Epilepsia (2013) 54 (1298-1306))', Epilepsia, vol. 54, no. 9, pp. 1709. https://doi.org/10.1111/epi.12384

Licchetta, L. ; Pippucci, T. ; Bisulli, F. ; Cantalupo, G. ; Magini, P. ; Alvisi, L. ; Baldassari, S. ; Martinelli, P. ; Naldi, I. ; Vanni, N. ; Liguori, R. ; Seri, M. ; Tinuper, P. / Erratum : A novel pedigree with familial cortical myoclonic tremor and epilepsy (FCMTE): Clinical characterization, refinement of the FCMTE2 locus, and confirmation of a founder haplotype (Epilepsia (2013) 54 (1298-1306)). In: Epilepsia. 2013 ; Vol. 54, No. 9. pp. 1709.

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Erratum: A novel pedigree with familial cortical myoclonic tremor and epilepsy (FCMTE): Clinical characterization, refinement of the FCMTE2 locus, and confirmation of a founder haplotype (Epilepsia (2013) 54 (1298-1306))

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