Clinical, hematologic and molecular variability of sickle cell-β thalassemia in western India

BACKGROUND: Sickle cell-β thalassemia (HbS-β thalassemia) is a sickling disorder of varying severity, which results from compound heterozygosity for sickle cell trait and β thalassemia trait. The present study was undertaken to determine the genetic factors responsible for the clinical variability o...

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Detalles Bibliográficos
Autores principales: Mukherjee, Malay B., Nadkarni, Anita H., Gorakshakar, Ajit C., Ghosh, Kanjaksha, Mohanty, Dipika, Colah, Roshan B.
Formato: Texto
Lenguaje:English
Publicado: Medknow Publications 2010
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3009427/
https://www.ncbi.nlm.nih.gov/pubmed/21206704
http://dx.doi.org/10.4103/0971-6866.73410

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3009427/
https://www.ncbi.nlm.nih.gov/pubmed/21206704
http://dx.doi.org/10.4103/0971-6866.73410

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