Low incidence of EPOR mutations in idiopathic erythrocytosis
- PMID: 32165487
- PMCID: PMC7776331
- DOI: 10.3324/haematol.2019.244160
Low incidence of EPOR mutations in idiopathic erythrocytosis
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References
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- Lenglet M, Robriquet F, Schwarz K, et al. Identification of a new VHL exon and complex splicing alterations in familial erythrocytosis or von Hippel-Lindau disease. Blood 2018;132(5):469-483. - PubMed
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