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The XmnI polymorphic site 5’ to the gene G(γ) in a Brazilian patient with sickle cell anaemia – fetal haemoglobin concentration, haematology and clinical features

We report a 20-year-old female with sickle cell anaemia and with an HbF concentration of 15.8%. The patient was not using hydroxyurea and was not receiving regular blood transfusions. The patient never had chronic manifestations of sickle cell anaemia, only pain crises of a mild intensity. After lab...

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Detalles Bibliográficos
Autores principales:	Belini Júnior, Édis, Cançado, Rodolfo D., Domingos, Claudia R.B.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Termedia Publishing House 2010
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3298355/ https://www.ncbi.nlm.nih.gov/pubmed/22419945 http://dx.doi.org/10.5114/aoms.2010.17101

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