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Peer Review reports

From: A rare c.183_187dupCTCAC mutation of the acetylcholine receptor CHRNE gene in a South Asian female with congenital myasthenic syndrome: a case report

Original Submission
4 Jul 2016 Submitted Original manuscript
Author responded Author comments
Reviewed Reviewer Report
Resubmission - Version 2
Submitted Manuscript version 2
Publishing
30 Sep 2016 Editorially accepted
7 Oct 2016 Article published 10.1186/s12883-016-0716-y

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BMC Neurology

ISSN: 1471-2377

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