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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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| Publicado en: | Int J Lab Hematol |
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| Autores principales: | , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
John Wiley and Sons Inc.
2018
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| Materias: | |
| Acceso en línea: | 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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