1.
Böckelmann LC, Basu T, Gründer A, Wang W, Breucker J, Kaiser S, Pichler A, Pahl HL. Concomitant constitutive LNK and NFE2 mutation with loss of sumoylation in a case of hereditary thrombocythemia. Haematologica [Internet]. 2021Apr.1 [cited 2026Nov.10];106(4):1158-62. Available from: https://haematologica.org/article/view/9788