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Erratum to Int. J. Mol. Sci. 2018, 19(11), 3675.
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Erratum

Correction: Sciacca, F. L., et al. Microduplication of 15q13.3 and Microdeletion of 18q21.32 in a Patient with Moyamoya Syndrome. Int. J. Mol. Sci. 2018, 19, 3675

by
Francesca Luisa Sciacca
1,
Ambra Rizzo
1,
Gloria Bedini
2,
Fioravante Capone
3,
Vincenzo Di Lazzaro
3,
Sara Nava
2,
Francesco Acerbi
4,
Davide Rossi Sebastiano
5,
Simona Binelli
5,
Giuseppe Faragò
6,
Andrea Gioppo
6,
Marina Grisoli
7,
Maria Grazia Bruzzone
7,
Paolo Ferroli
4,
Chiara Pantaleoni
8,
Luigi Caputi
9,
Jesus Vela Gomez
9,
Eugenio Agostino Parati
9 and
Anna Bersano
9,*
1
Dipartimento di Diagnostica e Tecnologia Applicata, Fondazione IRCCS Istituto Neurologico Carlo Besta, 20133 Milan, Italy
2
Laboratory of Cellular Neurobiology, Fondazione IRCCS Istituto Neurologico Carlo Besta, 20133 Milan, Italy
3
Unit of Neurology, Neurophysiology, Neurobiology, Department of Medicine, Università Campus Bio-Medico di Roma, 00128 Rome, Italy
4
Neurosurgical Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, 20133 Milan, Italy
5
Neurophysiopathology Department and Epilepsy Centre, Fondazione IRCCS Istituto Neurologico Carlo Besta, 20133 Milan, Italy
6
Interventional Neuroradiology Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, 20133 Milan, Italy
7
Neuroradiological Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, 20133 Milan, Italy
8
Developmental Neurology Division, Fondazione IRCCS Istituto Neurologico Carlo Besta, 20133 Milan, Italy
9
Cerebrovascular Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, 20133 Milan, Italy
*
Author to whom correspondence should be addressed.
Int. J. Mol. Sci. 2020, 21(1), 20; https://doi.org/10.3390/ijms21010020
Submission received: 19 November 2019 / Accepted: 21 November 2019 / Published: 18 December 2019
(This article belongs to the Section Molecular Neurobiology)
Versions Notes
The authors wish to make the corrections to this paper [1]. The surnames and names of all authors were switched in the original paper; the following being the right sequence: Francesca Luisa Sciacca, Ambra Rizzo, Gloria Bedini, Fioravante Capone, Vincenzo Di Lazzaro, Sara Nava, Francesco Acerbi, Davide Rossi Sebastiano, Simona Binelli, Giuseppe Faragò, Andrea Gioppo, Marina Grisoli, Maria Grazia Bruzzone, Paolo Ferroli, Chiara Pantaleoni, Luigi Caputi, Jesus Vela Gomez, Eugenio Agostino Parati and Anna Bersano.
The authors would like to apologize for any inconvenience caused to the readers by these changes.

Conflicts of Interest

The authors declare no conflict of interest.

Share and Cite

MDPI and ACS Style

Sciacca, F.L.; Rizzo, A.; Bedini, G.; Capone, F.; Di Lazzaro, V.; Nava, S.; Acerbi, F.; Sebastiano, D.R.; Binelli, S.; Faragò, G.; et al. Correction: Sciacca, F. L., et al. Microduplication of 15q13.3 and Microdeletion of 18q21.32 in a Patient with Moyamoya Syndrome. Int. J. Mol. Sci. 2018, 19, 3675. Int. J. Mol. Sci. 2020, 21, 20. https://doi.org/10.3390/ijms21010020

AMA Style

Sciacca FL, Rizzo A, Bedini G, Capone F, Di Lazzaro V, Nava S, Acerbi F, Sebastiano DR, Binelli S, Faragò G, et al. Correction: Sciacca, F. L., et al. Microduplication of 15q13.3 and Microdeletion of 18q21.32 in a Patient with Moyamoya Syndrome. Int. J. Mol. Sci. 2018, 19, 3675. International Journal of Molecular Sciences. 2020; 21(1):20. https://doi.org/10.3390/ijms21010020

Chicago/Turabian Style

Sciacca, Francesca Luisa, Ambra Rizzo, Gloria Bedini, Fioravante Capone, Vincenzo Di Lazzaro, Sara Nava, Francesco Acerbi, Davide Rossi Sebastiano, Simona Binelli, Giuseppe Faragò, and et al. 2020. "Correction: Sciacca, F. L., et al. Microduplication of 15q13.3 and Microdeletion of 18q21.32 in a Patient with Moyamoya Syndrome. Int. J. Mol. Sci. 2018, 19, 3675" International Journal of Molecular Sciences 21, no. 1: 20. https://doi.org/10.3390/ijms21010020

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