A limb-girdle myopathy phenotype of RUNX2 mutation in a patient with cleidocranial dysplasia: a case study and literature review
Pre-publication versions of this article are available by contacting firstname.lastname@example.org.
|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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