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A Novel Association of HbQ India Trait with Sickle Cell Anemia: a New Insight in Hemoglobinopathies

HbQ India is a rare α-chain structural hemoglobinopathy usually asymptomatic and presents in the heterozygous form or co-inherited with β-thalassemia trait. Herein, we are reporting the third case of novel association of HbQ India with HbS trait hemoglobinopathy in a 30-year-old young male presented...

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Detalles Bibliográficos
Autores principales:	Gupta, Rakesh K., Verma, Kartavya Kumar, Singh, Gurmeet
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Springer International Publishing 2022
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8723905/ https://www.ncbi.nlm.nih.gov/pubmed/35005433 http://dx.doi.org/10.1007/s42399-021-01103-y

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