Molecular genetic characterization of cblC defects in 126 pedigrees and prenatal genetic diagnosis of pedigrees with combined methylmalonic aciduria and homocystinuria
Pre-publication versions of this article are available by contacting firstname.lastname@example.org.
|2 Apr 2018||Submitted||Original manuscript|
|13 May 2018||Reviewed||Reviewer Report - Klaas Wierenga|
|24 May 2018||Reviewed||Reviewer Report - David Watkins|
|13 Jun 2018||Author responded||Author comments - Shuang Hu|
|Resubmission - Version 2|
|13 Jun 2018||Submitted||Manuscript version 2|
|6 Jul 2018||Reviewed||Reviewer Report - David Watkins|
|11 Aug 2018||Author responded||Author comments - Shuang Hu|
|Resubmission - Version 3|
|11 Aug 2018||Submitted||Manuscript version 3|
|15 Aug 2018||Editorially accepted|
|29 Aug 2018||Article published||10.1186/s12881-018-0666-x|
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