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Peer Review reports

From: Crigler-Najjar syndrome type II in a Chinese boy resulting from three mutations in the bilirubin uridine 5′-diphosphate-glucuronosyltransferase (UGT1A1) gene and a family genetic analysis

Original Submission
13 Aug 2014 Submitted Original manuscript
14 Aug 2014 Author responded Author comments - Zhifeng Liu
Resubmission - Version 2
14 Aug 2014 Submitted Manuscript version 2
19 Sep 2014 Reviewed Reviewer Report - Voranush Chongsrisawat
21 Sep 2014 Reviewed Reviewer Report - Nedeljko Radlovic
9 Oct 2014 Author responded Author comments - Zhifeng Liu
Resubmission - Version 3
9 Oct 2014 Submitted Manuscript version 3
Publishing
9 Oct 2014 Editorially accepted
15 Oct 2014 Article published 10.1186/1471-2431-14-267

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BMC Pediatrics

ISSN: 1471-2431

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