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Peer Review reports

From: Homozygous GRID2 missense mutation predicts a shift in the D-serine binding domain of GluD2 in a case with generalized brain atrophy and unusual clinical features

Original Submission
14 May 2017 Submitted Original manuscript
17 May 2017 Author responded Author comments - Niklas Dahl
Resubmission - Version 2
17 May 2017 Submitted Manuscript version 2
22 Jul 2017 Reviewed Reviewer Report - Hatem El-Shanti
28 Sep 2017 Reviewed Reviewer Report - Akihiko Kato
6 Oct 2017 Reviewed Reviewer Report - Naoto Hayasaka
24 Oct 2017 Author responded Author comments - Ali Zafar
Resubmission - Version 3
24 Oct 2017 Submitted Manuscript version 3
5 Nov 2017 Reviewed Reviewer Report - Hatem El-Shanti
5 Nov 2017 Reviewed Reviewer Report - Akihiko Kato
13 Nov 2017 Author responded Author comments - Zafar Ali
Resubmission - Version 4
13 Nov 2017 Submitted Manuscript version 4
Publishing
23 Nov 2017 Editorially accepted
6 Dec 2017 Article published 10.1186/s12881-017-0504-6

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