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From: A novel electron transfer flavoprotein dehydrogenase (ETFDH) gene mutation identified in a newborn with glutaric acidemia type II: a case report of a Chinese family

Original Submission
25 Mar 2019 Submitted Original manuscript
28 May 2019 Reviewed Reviewer Report - sara missaglia
11 Nov 2019 Reviewed Reviewer Report - Andrea Bordugo
12 Nov 2019 Reviewed Reviewer Report - Francesco Porta
12 Dec 2019 Author responded Author comments - Mingcai Ou
8 Mar 2020 Author responded Author comments - Mingcai Ou
Resubmission - Version 2
12 Dec 2019 Submitted Manuscript version 2
Publishing
10 Mar 2020 Editorially accepted
11 May 2020 Article published 10.1186/s12881-020-00995-2

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