A novel compound heterozygous mutation in VARS2 in a newborn with mitochondrial cardiomyopathy: a case report of a Chinese family
Pre-publication versions of this article are available by contacting firstname.lastname@example.org.
|11 Jun 2018||Submitted||Original manuscript|
|10 Jul 2018||Reviewed||Reviewer Report - Saskia Wortmann|
|3 Aug 2018||Reviewed||Reviewer Report - Costanza Lamperti|
|29 Aug 2018||Author responded||Author comments - Ning Li|
|Resubmission - Version 2|
|29 Aug 2018||Submitted||Manuscript version 2|
|20 Sep 2018||Editorially accepted|
|20 Nov 2018||Article published||10.1186/s12881-018-0689-3|
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