Molecular diagnosis of putative Stargardt disease probands by exome sequencing
© Strom et al.; licensee BioMed Central Ltd. 2012
Received: 11 April 2012
Accepted: 25 July 2012
Published: 3 August 2012
Open Peer Review reports
Pre-publication versions of this article and author comments to reviewers are available by contacting email@example.com.
|11 Apr 2012||Submitted||Original manuscript|
|Resubmission - Version 2|
|Submitted||Manuscript version 2|
|13 May 2012||Reviewed||Reviewer Report - Rando Allikmets|
|28 May 2012||Reviewed||Reviewer Report - Stephen Tsang|
|22 Jun 2012||Author responded||Author comments - Samuel Strom|
|Resubmission - Version 3|
|22 Jun 2012||Submitted||Manuscript version 3|
|10 Jul 2012||Reviewed||Reviewer Report - Rando Allikmets|
|Resubmission - Version 4|
|Submitted||Manuscript version 4|
|25 Jul 2012||Editorially accepted|
|3 Aug 2012||Article published||10.1186/1471-2350-13-67|
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