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Peer Review reports

From: Novel homozygous missense mutation in GAN associated with Charcot-Marie-Tooth disease type 2 in a large consanguineous family from Israel

Original Submission
10 Jun 2016 Submitted Original manuscript
Author responded Author comments
Reviewed Reviewer Report
Resubmission - Version 2
Submitted Manuscript version 2
Publishing
7 Nov 2016 Editorially accepted
16 Nov 2016 Article published 10.1186/s12881-016-0343-x

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BMC Medical Genetics

ISSN: 1471-2350

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