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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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Detalles Bibliográficos
Autores principales:	Dadheech, Sneha, Madhulatha, D., Jain, Suman, Joseph, James, Jyothy, A., Munshi, Anjana
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Medknow Publications & Media Pvt Ltd 2016
Materias:	Original Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4928551/ https://www.ncbi.nlm.nih.gov/pubmed/27377501 http://dx.doi.org/10.4103/0971-5916.184285

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