Response to: “Heterogeneous phenotypic expression of C1QBP variants is
attributable to variable heteroplasmy of secondary mtDNA deletions and
mtDNA copy number”
- Costanza Lamperti,
- Silvia Marchet,
- Andrea Legati,
- Daniele Ghezzi
Costanza Lamperti
Fondazione IRCCS Istituto Neurologico Carlo Besta
Corresponding Author:costanza.lamperti@istituto-besta.it
Author ProfileSilvia Marchet
Fondazione IRCCS Istituto Neurologico Carlo Besta
Author ProfileAndrea Legati
Fondazione IRCCS Istituto Neurologico Carlo Besta
Author ProfileDaniele Ghezzi
Fondazione IRCCS Istituto Neurologico Carlo Besta
Author Profile31 Aug 2020Submitted to Human Mutation 01 Sep 2020Submission Checks Completed
01 Sep 2020Assigned to Editor
01 Sep 2020Review(s) Completed, Editorial Evaluation Pending
01 Sep 2020Reviewer(s) Assigned
02 Oct 2020Editorial Decision: Accept
Nov 2020Published in Human Mutation volume 41 issue 11 on pages 2014-2015. 10.1002/humu.24122 
