Clinical features and genetic analysis of two siblings with startle disease in an Italian family: a case report
Pre-publication versions of this article are available by contacting firstname.lastname@example.org.
|2 Jan 2019||Submitted||Original manuscript|
|28 Jan 2019||Reviewed||Reviewer Report - Amrik Sahota|
|12 Feb 2019||Reviewed||Reviewer Report - Éliane Chouery|
|13 Feb 2019||Author responded||Author comments - Teresa Sprovieri|
|Resubmission - Version 2|
|13 Feb 2019||Submitted||Manuscript version 2|
|28 Feb 2019||Author responded||Author comments - Teresa Sprovieri|
|Resubmission - Version 3|
|28 Feb 2019||Submitted||Manuscript version 3|
|6 Mar 2019||Editorially accepted|
|12 Mar 2019||Article published||10.1186/s12881-019-0779-x|
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