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Clinical, hematologic and molecular variability of sickle cell-β thalassemia in western India
BACKGROUND: Sickle cell-β thalassemia (HbS-β thalassemia) is a sickling disorder of varying severity, which results from compound heterozygosity for sickle cell trait and β thalassemia trait. The present study was undertaken to determine the genetic factors responsible for the clinical variability o...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Medknow Publications
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3009427/ https://ncbi.nlm.nih.gov/pubmed/21206704 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0971-6866.73410 |
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