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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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Bibliografski detalji
Izdano u:Indian J Med Res
Glavni autori: Dadheech, Sneha, Madhulatha, D., Jain, Suman, Joseph, James, Jyothy, A., Munshi, Anjana
Format: Artigo
Jezik:Inglês
Izdano: Medknow Publications & Media Pvt Ltd 2016
Teme:
Online pristup: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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