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Peer Review reports

From: Whole-exome sequencing identifies homozygous mutation in TTI2 in a child with primary microcephaly: a case report

Original Submission
23 Dec 2019 Submitted Original manuscript
24 Jan 2020 Author responded Author comments - Vincent Picher-Martel
7 Feb 2020 Author responded Author comments - Vincent Picher-Martel
12 Jan 2020 Reviewed Reviewer Report - Ni-Chung Lee
15 Jan 2020 Reviewed Reviewer Report - Taku Hatano
5 Feb 2020 Reviewed Reviewer Report - Ni-Chung Lee
28 Jan 2020 Reviewed Reviewer Report - Taku Hatano
Resubmission - Version 2
24 Jan 2020 Submitted Manuscript version 2
Publishing
12 Feb 2020 Editorially accepted
15 Feb 2020 Article published 10.1186/s12883-020-01643-1

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