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Peer Review reports

From: Arthropathy-related pain in a patient with congenital impairment of pain sensation due to hereditary sensory and autonomic neuropathy type II with a rare mutation in the WNK1/HSN2 gene: a case report

Original Submission
13 Apr 2016 Submitted Original manuscript
Author responded Author comments
Reviewed Reviewer Report
Resubmission - Version 2
Submitted Manuscript version 2
Author responded Author comments
Reviewed Reviewer Report
Resubmission - Version 3
Submitted Manuscript version 3
Publishing
15 Oct 2016 Editorially accepted
21 Oct 2016 Article published 10.1186/s12883-016-0727-8

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BMC Neurology

ISSN: 1471-2377

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