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Peer Review reports

From: Functional validation of novel compound heterozygous variants in B3GAT3 resulting in severe osteopenia and fractures: expanding the disease phenotype

Original Submission
22 Jun 2016 Submitted Original manuscript
Author responded Author comments
Reviewed Reviewer Report
Resubmission - Version 2
Submitted Manuscript version 2
Author responded Author comments
Resubmission - Version 3
Submitted Manuscript version 3
Publishing
6 Nov 2016 Editorially accepted
21 Nov 2016 Article published 10.1186/s12881-016-0344-9

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BMC Medical Genetics

ISSN: 1471-2350

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