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A novel mutation in the ABCD1 gene of a Moroccan patient with X-linked adrenoleukodystrophy: case report

  • Adnane Karkar1, 2,
  • Abdelhamid Barakat3,
  • Amina Bakhchane3,
  • Houda Fettah4,
  • Ilham Slassi5,
  • Imen Dorboz6,
  • Odile Boespflug-Tanguy6, 7 and
  • Sellama Nadifi2Email author
BMC Neurology201515:244

https://doi.org/10.1186/s12883-015-0503-1

Received: 6 August 2015

Accepted: 21 November 2015

Published: 25 November 2015

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Open Peer Review reports

Pre-publication versions of this article are available by contacting info@biomedcentral.com.

Original Submission
6 Aug 2015 Submitted Original manuscript
21 Sep 2015 Reviewed Reviewer Report - Fakhri Kallabi
12 Oct 2015 Reviewed Reviewer Report - Ginevra Zanni
6 Nov 2015 Author responded Author comments - Adnane Karkar
Resubmission - Version 2
6 Nov 2015 Submitted Manuscript version 2
19 Nov 2015 Author responded Author comments - Adnane Karkar
Resubmission - Version 3
19 Nov 2015 Submitted Manuscript version 3
Publishing
21 Nov 2015 Editorially accepted
25 Nov 2015 Article published 10.1186/s12883-015-0503-1

How does Open Peer Review work?

Open peer review is a system where authors know who the reviewers are, and the reviewers know who the authors are. If the manuscript is accepted, the named reviewer reports are published alongside the article. Pre-publication versions of the article are available by contacting info@biomedcentral.com.

You can find further information about the peer review system here.

Authors’ Affiliations

(1)
Inserm U1141, Paris Diderot University, Sorbonne Paris Cité, Robert Debré Hospital, Paris, France
(2)
Genetics and Molecular Pathology Laboratory, Medical school of Casablanca, Hassan II University, Casablanca, Morocco
(3)
Laboratoire de Génétique Moléculaire Humaine, Département de la Recherche Scientifique, Institut Pasteur du Maroc, Casablanca, Morocco
(4)
Department of Neuropediatrics, Hassan II University Hospital, Casablanca, Morocco
(5)
Department of Neurology, Hassan II University Hospital, Casablanca, Morocco
(6)
Inserm U1141, Paris Diderot University, Sorbonne Paris Cité, DHU PROTECT, Robert Debré Hospital, Paris, France
(7)
Reference Center For Leukodystrophies, Department of Neuropediatrics and Metabolic Diseases, Robert Debré Hospital, AP-HP, Paris, France

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