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This article has Open Peer Review reports available.

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De novo p.Arg756Cys mutation of ATP1A3 causes an atypical form of alternating hemiplegia of childhood with prolonged paralysis and choreoathetosis

  • 1,
  • 2,
  • 1Email author,
  • 1,
  • 2,
  • 1, 3,
  • 1,
  • 1,
  • 1,
  • 1,
  • 1,
  • 1, 4,
  • 2, 5,
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  • 1, 3
Contributed equally
BMC NeurologyBMC series – open, inclusive and trusted201616:174

https://doi.org/10.1186/s12883-016-0680-6

Received: 16 March 2016

Accepted: 26 August 2016

Published: 15 September 2016

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Open Peer Review reports

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

Original Submission
16 Mar 2016 Submitted Original manuscript
Author responded Author comments
Reviewed Reviewer Report
Resubmission - Version 2
Submitted Manuscript version 2
Author responded Author comments
Reviewed Reviewer Report
Resubmission - Version 3
Submitted Manuscript version 3
Publishing
26 Aug 2016 Editorially accepted
15 Sep 2016 Article published 10.1186/s12883-016-0680-6

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)
Department of Pediatrics, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan
(2)
Department of Human Genetics, Yokohama City University School of Medicine, Yokohama, Japan
(3)
Present address: Fukuoka Children’s Hospital, Fukuoka, Japan
(4)
Present address: Section of Pediatrics, Department of Medicine, Fukuoka Dental College, Fukuoka, Japan
(5)
Present address: Department of Biochemistry, Hamamatsu University School of Medicine, Hamamatsu, Japan

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