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Open Access

Correction to: Exome sequencing reveals a novel PLP1 mutation in a Moroccan family with connatal Pelizaeus-Merzbacher disease: a case report

  • Jaber Lyahyai1Email author,
  • Bouchra Ouled Amar Bencheikh2, 3,
  • Siham C. Elalaoui4,
  • Maria Mansouri1, 4,
  • Lamia Boualla1,
  • Alexandre DIonne-Laporte2, 3,
  • Dan Spiegelman2, 3,
  • Patrick A. Dion2, 3,
  • Patrick Cossette5,
  • Guy A. Rouleau2, 3 and
  • Abdelaziz Sefiani1, 4
BMC PediatricsBMC series – open, inclusive and trusted201818:138

https://doi.org/10.1186/s12887-018-1114-y

Published: 17 April 2018

The original article was published in BMC Pediatrics 2018 18:90

Correction

After publication of the original article [1] it was brought to our attention that author Bouchra Ouled Amar Bencheikh was incorrectly included as Bouchra Oulad Amar Bencheikh.

The correct spelling of the name is included in the author list of this ‘Correction’ and updated in the original article.

Notes

Declarations

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Authors’ Affiliations

(1)
Centre de Génomique Humaine, Faculté de Médecine et Pharmacie, Mohammed V University in Rabat, Rabat, Morocco
(2)
Montreal Neurological Institute and Hospital, Montreal, Canada
(3)
Department of Neurology and Neurosurgery, McGill University, Montreal, Canada
(4)
Département de Génétique Médicale, Institut National d’Hygiène, Rabat, Morocco
(5)
Molecular Diagnostic Laboratory and Division of Medical Genetics, CHU Sainte-Justine, Montreal, Canada

Reference

  1. Lyahyai J, et al. Exome sequencing reveals a novel PLP1 mutation in a Moroccan family with connatal Pelizaeus-Merzbacher disease: a case report. BMC Pediatr. 2018;18:90. https://doi.org/10.1186/s12887-018-1063-5.View ArticlePubMedPubMed CentralGoogle Scholar

Copyright

© The Author(s). 2018

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