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Peer Review reports

From: Whole-exome sequencing and digital PCR identified a novel compound heterozygous mutation in the NPHP1 gene in a case of Joubert syndrome and related disorders

Original Submission
21 Jun 2016 Submitted Original manuscript
2 Jan 2017 Reviewed Reviewer Report - Ji Eun Lee
5 Jan 2017 Reviewed Reviewer Report - Alistair Pagnamenta
3 Feb 2017 Author responded Author comments - Shingo Koyama
Resubmission - Version 2
3 Feb 2017 Submitted Manuscript version 2
3 Mar 2017 Reviewed Reviewer Report - Alistair Pagnamenta
12 Mar 2017 Author responded Author comments - Shingo Koyama
Resubmission - Version 3
12 Mar 2017 Submitted Manuscript version 3
Publishing
14 Mar 2017 Editorially accepted
27 Mar 2017 Article published 10.1186/s12881-017-0399-2

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BMC Medical Genetics

ISSN: 1471-2350

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