Concomitant constitutive LNK and NFE2 mutation with loss of sumoylation in a case of hereditary thrombocythemia.

Concomitant constitutive LNK and NFE2 mutation with loss of sumoylation in a case of hereditary thrombocythemia. Haematologica. 2020 Jun 18;: Authors: Böckelmann LC, Basu T, Gründer A, Wang W, Breucker J, Kaiser S, Pichler A, Pahl HL PMID: 32554556 [PubMed - as supplied by publisher]

https://www.ncbi.nlm.nih.gov/pubmed/32554556?dopt=Abstract

Source: Haematologica - June 17, 2020 Category: Hematology Authors: Böckelmann LC, Basu T, Gründer A, Wang W, Breucker J, Kaiser S, Pichler A, Pahl HL Tags: Haematologica Source Type: research

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