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Peer Review reports

From: A Japanese case of oculopharyngeal muscular dystrophy (OPMD) with PABPN1 c.35G > C; p.Gly12Ala point mutation

Original Submission
17 May 2021 Submitted Original manuscript
14 Jun 2021 Reviewed Reviewer Report
18 Jun 2021 Reviewed Reviewer Report
23 Jun 2021 Author responded Author comments - Yo-suke Nishii
Resubmission - Version 2
23 Jun 2021 Submitted Manuscript version 2
Publishing
25 Jun 2021 Editorially accepted
5 Jul 2021 Article published 10.1186/s12883-021-02300-x

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