Work

UPD1p indicates the presence of MPL W515L mutation in RARS-T, a mechanism analogous to UPD9p and JAK2 V617F mutation

Year: 2008

Type: article

Source: Leukemia

DOI: 10.1038/leu.2008.249

Authors: H Szpurka, L P Gondek, S R Mohan, E D Hsi, K S Theil, J P Maciejewski

Institution: Cleveland Clinic

Language: English

Topic: Myeloproliferative Neoplasms: Diagnosis and Treatment

Subfield: Genetics

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: closed

Funders: National Institutes of Health, National Heart, Lung, and Blood Institute, National Center for Research Resources

Awards: G2564966186, G481402874, Training/Research Center-Bone Marrow Failure Syndromes, Predisposition to chromosomal alterations in MDS

OpenAlex ID: W1964295470

FWCI: 3.98

Cites: 8

Cited by: 49

Related to: 10