Jørgensen, Silje F.
Buechner, Jochen
Myhre, Anders E.
Galteland, Eivind
Spetalen, Signe
Kulseth, Mari Ann
Sorte, Hanne S.
Holla, Øystein L.
Lundman, Emma
Alme, Charlotte
Heier, Ingvild
Flægstad, Trond
Fløisand, Yngvar
Benneche, Andreas
Fevang, Børre
Aukrust, Pål
Stray-Pedersen, Asbjørg
Gedde-Dahl, Tobias
Nordøy, Ingvild
Funding for this research was provided by:
University of Oslo
Article History
Received: 12 May 2021
Accepted: 29 November 2021
First Online: 10 December 2021
Declarations
:
: Five of the patients had previously consented to be part of a genetic PID research project approved by the regional ethical committee (REC. 2014/1270–1), three patients were diagnosed with MDS in childhood and consented to be registered into the EWOG-MDS-2006 study (2015/1651/REC Nord), and all adult patients who underwent allo-HSCT had consented to publication of data (REC 11909). Studies were performed according to the Declaration of Helsinki.
: All adult living patients signed a written informed consent for publication. For children < 18 years, consent was given by their parents.
: Obtained.
: The authors declare no competing interests.