Mitochondrial DNA variant m.15218A > G in Finnish epilepsy patients who have maternal relatives with epilepsy, sensorineural hearing impairment or diabetes mellitus
Pre-publication versions of this article are available by contacting email@example.com.
|25 Sep 2012||Submitted||Original manuscript|
|17 Dec 2012||Reviewed||Reviewer Report - Gabor Zsurka|
|20 Dec 2012||Reviewed||Reviewer Report - Haris Kokotas|
|28 Dec 2012||Reviewed||Reviewer Report - Elena Cardaioli|
|25 Mar 2013||Author responded||Author comments - Heidi Soini|
|Resubmission - Version 2|
|25 Mar 2013||Submitted||Manuscript version 2|
|24 May 2013||Reviewed||Reviewer Report - Gabor Zsurka|
|Resubmission - Version 3|
|Submitted||Manuscript version 3|
|17 Jul 2013||Editorially accepted|
|19 Jul 2013||Article published||10.1186/1471-2350-14-73|
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