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Genetic variants of erythropoietin (EPO) and EPO receptor genes in familial erythrocytosis

OBJECTIVES: Erythrocytosis is characterized by the expansion of erythrocyte compartment including elevated red blood cell number, hematocrit, and hemoglobin content. Familial erythrocytosis (FE) is a congenital disorder with different genetic background. Type 1 FE is primary FE caused by mutation in...

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Dades bibliogràfiques
Publicat a:Int J Lab Hematol
Autors principals: Vočanec, Danijela, Prijatelj, Tinkara, Debeljak, Nataša, Kunej, Tanja
Format: Artigo
Idioma:Inglês
Publicat: John Wiley and Sons Inc. 2018
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC7379665/
https://ncbi.nlm.nih.gov/pubmed/30507031
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/ijlh.12949
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