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Peer Review reports

From: Leber’s hereditary optic neuropathy, intellectual disability and epilepsy presenting with variable penetrance associated to the m.3460G >A mutation and a heteroplasmic expansion of the microsatellite in MTRNR1 gene – case report

Original Submission
9 Feb 2018 Submitted Original manuscript
27 Mar 2018 Reviewed Reviewer Report - Filippo M. Santorelli
27 Apr 2018 Reviewed Reviewer Report - Carlos Moraes
31 May 2018 Author responded Author comments - Vittoria Petruzzella
Resubmission - Version 2
31 May 2018 Submitted Manuscript version 2
18 Jun 2018 Author responded Author comments - Vittoria Petruzzella
Resubmission - Version 3
18 Jun 2018 Submitted Manuscript version 3
6 Jul 2018 Author responded Author comments - Vittoria Petruzzella
Resubmission - Version 4
6 Jul 2018 Submitted Manuscript version 4
Publishing
12 Jul 2018 Editorially accepted
27 Jul 2018 Article published 10.1186/s12881-018-0644-3

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BMC Medical Genetics

ISSN: 1471-2350

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