A novel homozygous mutation in the glycerol-3-phosphate dehydrogenase 1 gene in a Chinese patient with transient infantile hypertriglyceridemia: a case report
Pre-publication versions of this article are available by contacting firstname.lastname@example.org.
|10 Feb 2018||Submitted||Original manuscript|
|13 Mar 2018||Reviewed||Reviewer Report - Somaya Albhaisi|
|21 Mar 2018||Reviewed||Reviewer Report - Alisan Kahraman|
|6 Apr 2018||Reviewed||Reviewer Report - Andreas Maieron|
|5 May 2018||Author responded||Author comments - Jia-Qi Li|
|Resubmission - Version 2|
|5 May 2018||Submitted||Manuscript version 2|
|21 May 2018||Reviewed||Reviewer Report - Andreas Maieron|
|18 Jun 2018||Author responded||Author comments - Jia-Qi Li|
|Resubmission - Version 3|
|18 Jun 2018||Submitted||Manuscript version 3|
|19 Jun 2018||Editorially accepted|
|25 Jun 2018||Article published||10.1186/s12876-018-0827-6|
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