Mucopolysaccharidosis IIIB and mild skeletal anomalies: coexistence of NAGLU and CYP26B1 missense variations in the same patient in a Chinese family

Peer Review reports

Original Submission
12 Dec 2017	Submitted	Original manuscript
18 Jan 2018	Reviewed	Reviewer Report - Shunji Tomatsu
24 Jan 2018	Reviewed	Reviewer Report - Orazio Gabrielli
10 Feb 2018	Author responded	Author comments - Jinliang Li
Resubmission - Version 2
10 Feb 2018	Submitted	Manuscript version 2
11 Mar 2018	Author responded	Author comments - Jinliang Li
Resubmission - Version 3
11 Mar 2018	Submitted	Manuscript version 3
Publishing
19 Mar 2018	Editorially accepted
2 Apr 2018	Article published	10.1186/s12881-018-0562-4

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