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Peer Review reports

From: Compound heterozygous POMGNT1 mutations leading to muscular dystrophy-dystroglycanopathy type A3: a case report

Original Submission
26 Aug 2018 Submitted Original manuscript
28 Dec 2018 Reviewed Reviewer Report - Raffaele Falsaperla
12 Feb 2019 Reviewed Reviewer Report - Reviewer 2
15 Mar 2019 Author responded Author comments - Olga Borisovna Kondakova
Resubmission - Version 2
15 Mar 2019 Submitted Manuscript version 2
Publishing
24 Mar 2019 Editorially accepted
8 Apr 2019 Article published 10.1186/s12887-019-1470-2

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