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Peer Review reports

From: A limb-girdle myopathy phenotype of RUNX2 mutation in a patient with cleidocranial dysplasia: a case study and literature review

Original Submission
24 Aug 2016 Submitted Original manuscript
27 Sep 2016 Reviewed Reviewer Report - Umesh Badrising
2 Oct 2016 Reviewed Reviewer Report - Klary E. Niezen-Koning
15 Oct 2016 Author responded Author comments - Sung-Ju Hsueh
Resubmission - Version 2
15 Oct 2016 Submitted Manuscript version 2
7 Dec 2016 Editorially accepted
6 Jan 2017 Article published 10.1186/s12883-016-0781-2

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