This article has Open Peer Review reports available.
A novel frameshift GRN mutation results in frontotemporal lobar degeneration with a distinct clinical phenotype in two siblings: case report and literature review
- Takashi Hosaka†1,
- Kazuhiro Ishii†1Email author,
- Takeshi Miura2, 3,
- Naomi Mezaki2, 3,
- Kensaku Kasuga2,
- Takeshi Ikeuchi2 and
- Akira Tamaoka1
© The Author(s). 2017
Received: 24 May 2017
Accepted: 1 September 2017
Published: 15 September 2017
Open Peer Review reports
Pre-publication versions of this article and author comments to reviewers are available by contacting email@example.com.
|24 May 2017||Submitted||Original manuscript|
|23 Jun 2017||Reviewed||Reviewer Report - Daniela Galimberti|
|28 Jun 2017||Reviewed||Reviewer Report - David Weidman|
|18 Jul 2017||Author responded||Author comments - Takashi Hosaka|
|Resubmission - Version 2|
|18 Jul 2017||Submitted||Manuscript version 2|
|24 Jul 2017||Reviewed||Reviewer Report - Daniela Galimberti|
|28 Jul 2017||Reviewed||Reviewer Report - David Weidman|
|14 Aug 2017||Author responded||Author comments - Takashi Hosaka|
|Resubmission - Version 3|
|14 Aug 2017||Submitted||Manuscript version 3|
|1 Sep 2017||Editorially accepted|
|15 Sep 2017||Article published||10.1186/s12883-017-0959-2|
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