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Modulating Effect of the −158 (G)γ (C→T) Xmn1 Polymorphism in Indian Sickle Cell Patients

Xmn1 polymorphism is a known factor, which increases fetal haemoglobin production. Among the inherited disorders of blood, thalassaemia and Sickle Cell Diseases contributes to a major bulk of genetic diseases in India. Our aim was to verify the role of the Xmn1 polymorphism as a modulating factor in...

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Detalles Bibliográficos
Autores principales:	Pandey, Sanjay, Pandey, Sweta, Mishra, Rahasya Mani, Saxena, Renu
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Università Cattolica del Sacro Cuore 2012
Materias:	Original Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3279316/ https://www.ncbi.nlm.nih.gov/pubmed/22348183 http://dx.doi.org/10.4084/MJHID.2012.001

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