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Phenotypic Effect of α‐Globin Gene Numbers on Indian Sickle β‐Thalassemia Patients
BACKGROUND: Sickle cell β‐thalassemia is a compound heterozygous state of β‐thalassemia and sickle cell anemia. Patient with these conditions showed mild‐to‐severe clinical phenotype. OBJECTIVES: The objective of this study was to evaluate the effects of α‐globin gene numbers on the phenotype of sic...
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| Publicat a: | J Clin Lab Anal |
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| Autors principals: | , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
John Wiley and Sons Inc.
2014
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6807439/ https://ncbi.nlm.nih.gov/pubmed/24395608 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jcla.21652 |
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