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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Detalles Bibliográficos
Autores principales: Vočanec, Danijela, Prijatelj, Tinkara, Debeljak, Nataša, Kunej, Tanja
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Review Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7379665/
https://www.ncbi.nlm.nih.gov/pubmed/30507031
http://dx.doi.org/10.1111/ijlh.12949

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7379665/
https://www.ncbi.nlm.nih.gov/pubmed/30507031
http://dx.doi.org/10.1111/ijlh.12949

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