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Association of BCL11A genetic variant (rs11886868) with severity in β-thalassaemia major & sickle cell anaemia
BACKGROUND & OBJECTIVES: The amount of foetal haemoglobin that persists in adulthood affects the clinical severity of haemoglobinopathies including β-thalassaemia major and sickle cell anaemia (SCA). The present study was undertaken to analyse β-thalassaemia as well as SCA patients for the singl...
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| Publicado no: | Indian J Med Res |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Medknow Publications & Media Pvt Ltd
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4928551/ https://ncbi.nlm.nih.gov/pubmed/27377501 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0971-5916.184285 |
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