Condition: Sickle cell-Hemoglobin O Arab disease
rs33946267 in
HBB gene and
Sickle cell-Hemoglobin O Arab disease
PMID 9834244 1998 HbS-oman heterozygote: a new dominant sickle syndrome.
PMID 3859465 1985 The interaction of hemoglobin O Arab with Hb S and beta+ thalassemia among Israeli Arabs.
PMID 11179419 2001 Characterization of syntenin, a syndecan-binding PDZ protein, as a component of cell adhesion sites and microfilaments.
PMID 22975760 2013 An empirical estimate of carrier frequencies for 400+ causal Mendelian variants: results from an ethnically diverse clinical sample of 23,453 individuals.
PMID 5481775 1970 Hemoglobin O arab in four negro families and its interaction with hemoglobin S and hemoglobin C.
PMID 24880717 2014 Molecular diagnostics of the HBB gene in an Omani cohort using bench-top DNA Ion Torrent PGM technology.
PMID 1732017 1992 Hemoglobin variants and activity of the (K+Cl-) cotransport system in human erythrocytes.
PMID 1112610 1975 Twelve families with Hb O Arab in the Burgas district of Bulgaria. Observations on sixteen examples of Hb O Arab-beta (0) thalassaemia.