Cargando…
The Properties of Red Blood Cells from Patients Heterozygous for HbS and HbC (HbSC Genotype)
Sickle cell disease (SCD) is one of the commonest severe inherited disorders, but specific treatments are lacking and the pathophysiology remains unclear. Affected individuals account for well over 250,000 births yearly, mostly in the Tropics, the USA, and the Caribbean, also in Northern Europe as w...
Autores principales: | Hannemann, A., Weiss, E., Rees, D. C., Dalibalta, S., Ellory, J. C., Gibson, J. S. |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3066570/ https://www.ncbi.nlm.nih.gov/pubmed/21490760 http://dx.doi.org/10.1155/2011/248527 |
Ejemplares similares
-
Cation Homeostasis in Red Cells From Patients With Sickle Cell Disease Heterologous for HbS and HbC (HbSC Genotype)
por: Hannemann, A., et al.
Publicado: (2015) -
Haemoglobin C Promotes Distinct Membrane Properties in Heterozygous HbSC red Cells
por: Clive Ellory, J.
Publicado: (2015) -
Retinal thickness measurements in sickle cell patients with HbSS and HbSC genotype
por: Lim, Wei S., et al.
Publicado: (2018) -
Sickle cell disease: A distinction of two most frequent genotypes (HbSS and HbSC)
por: da Guarda, Caroline Conceição, et al.
Publicado: (2020) -
Genome wide association study of silent cerebral infarction in sickle cell disease (HbSS and HbSC)
por: Brewin, John N., et al.
Publicado: (2020)