A more extensive analysis of the EPOgene in case of a suspected hereditary erythrocytosis will en-able the establishment of a more accurate diagnosis of patients,regardless of serum EPO levels.

Characterization of a Newly Discovered Non-Coding Variant in the EPO Gene Identified in Two Unrelated Italian Pedigrees With Erythrocytosis

Borsani, O;Rumi, E;
2026-01-01

Abstract

A more extensive analysis of the EPOgene in case of a suspected hereditary erythrocytosis will en-able the establishment of a more accurate diagnosis of patients,regardless of serum EPO levels.
2026
The Hematology category covers resources concerned with blood, blood-forming tissues, bone marrow, plasma, and transfusions. Coverage also includes resources on specialties such as hemophilia, leukemia, and lymphoma.
Esperti anonimi
Inglese
Internazionale
ELETTRONICO
101
4
894
898
5
erythrocytosis, erythropoietin, mutation
https://pubmed.ncbi.nlm.nih.gov/41708977/
no
11
info:eu-repo/semantics/article
262
Mora, B; Bellani, V; Pietra, D; Tagliaferri, E; Cattaneo, D; Borsani, O; Iurlo, A; Fermo, E; Bianchi, P; Rumi, E; Passamonti, F
1 Contributo su Rivista::1.1 Articolo in rivista
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11571/1545522
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