Funding for this research was provided by:
Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico (RC 2019-2020, PED-CARE-2018)
Received: 23 November 2020
Accepted: 19 March 2021
First Online: 31 March 2021
: This work is part of the “CARE: Challenging Approaches to undiagnosed Rare diseases with exome sequencing” Project (Protocol code: PED-CARE-2018).Appropriate written informed consent was obtained from all family members.
: Appropriate written informed consent was obtained for publication.
: The authors declare that they have no competing interests.