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

Peer Review reports

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
Publishing
7 Dec 2016	Editorially accepted
6 Jan 2017	Article published	10.1186/s12883-016-0781-2

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