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Cytogenetics and Cell Genetics|January 1, 1992
Assignment of the chromosomal locus of the human 30-kDal Rh (rhesus) blood group-antigen-related protein (Rh30A) to chromosome region 1p36.13----p34C MacGeoch, C J Mitchell, B Carritt, et al.
The Journal of Biological Chemistry|June 14, 1996
Immunochemical analysis of the human erythrocyte Rh polypeptidesN D Avent, W Liu, K M Warner, et al.
Transfusion Medicine (Oxford, England)|June 3, 1999
Glycophorin A mutation Ala65 --> Pro gives rise to a novel pair of MNS alleles ENEP (MNS39) and HAG (MNS41) and altered Wrb expression: direct evidence for GPA/band 3 interaction necessary for normal Wrb expressionJ Poole, J Banks, L J Bruce, et al.
Blood|December 15, 1991
Biochemical studies on red blood cells from a patient with the Inab phenotype (decay-accelerating factor deficiency)M E Reid, G Mallinson, R B Sim, et al.
Transfusion|May 29, 2000
The low-frequency MNS blood group antigens Ny(a) (MNS18) and Os(a) (MNS38) are associated with GPA amino acid substitutionsG L Daniels, L J Bruce, W J Mawby, et al.
British Journal of Haematology|January 1, 1997
Novel band 3 variants (bands 3 Foggia, Napoli I and Napoli II) associated with hereditary spherocytosis and band 3 deficiency: status of the D38A polymorphism within the EPB3 locusE Miraglia del Giudice, A Vallier, P Maillet, et al.
Blood|April 21, 2001
Glycophorin A dimerization and band 3 interaction during erythroid membrane biogenesis: in vivo studies in human glycophorin A transgenic miceI Auffray, S Marfatia, K de Jong, et al.
British Journal of Haematology|April 1, 1995
A point mutation in the protein 4.2 gene (allele 4.2 Tozeur) associated with hereditary haemolytic anaemiaS Hayette, L Morle, M Bozon, et al.
British Journal of Haematology|December 1, 1995
Band 3 Chur: a variant associated with band 3-deficient hereditary spherocytosis and substitution in a highly conserved position of transmembrane segment 11P Maillet, A Vallier, W H Reinhart, et al.
The Journal of Clinical Investigation|October 6, 1997
Familial distal renal tubular acidosis is associated with mutations in the red cell anion exchanger (Band 3, AE1) geneL J Bruce, D L Cope, G K Jones, et al.
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