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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
- Zafar Ali†1, 2,
- Shumaila Zulfiqar†1,
- Joakim Klar†1,
- Johan Wikström3,
- Farid Ullah2,
- Ayaz Khan2,
- Uzma Abdullah2,
- Shahid Baig2 and
- Niklas Dahl1Email authorView ORCID ID profile
© The Author(s). 2017
Received: 14 May 2017
Accepted: 23 November 2017
Published: 6 December 2017
Open Peer Review reports
Pre-publication versions of this article and author comments to reviewers are available by contacting firstname.lastname@example.org.
|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|
|23 Nov 2017||Editorially accepted|
|6 Dec 2017||Article published||10.1186/s12881-017-0504-6|
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