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Peer Review reports

From: Identification and in silico characterization of a novel p.P208PfsX1 mutation in V-ATPase a3 subunit associated with autosomal recessive osteopetrosis in a Pakistani family

Original Submission
11 Aug 2017 Submitted Original manuscript
11 Sep 2017 Reviewed Reviewer Report - Petra Henning
31 Oct 2017 Author responded Author comments - Muhammad Ajmal
Resubmission - Version 2
31 Oct 2017 Submitted Manuscript version 2
8 Nov 2017 Reviewed Reviewer Report - Petra Henning
22 Nov 2017 Author responded Author comments - Muhammad Ajmal
Resubmission - Version 3
22 Nov 2017 Submitted Manuscript version 3
Publishing
29 Nov 2017 Editorially accepted
13 Dec 2017 Article published 10.1186/s12881-017-0506-4

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BMC Medical Genetics

ISSN: 1471-2350

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