The KEL24 and KEL14 alleles of the Kell blood group system

Transfusion

Volumn 37, Issue 10, 1997, Pages 1035-1038

  Lee, S ^a   Naime, D ^a   Reid, M ^a   Redman, C ^a  

^a NEW YORK BLOOD CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; AMINO ACID SUBSTITUTION; ANTIGEN EXPRESSION; ARTICLE; BLOOD GROUP KELL SYSTEM; ERYTHROCYTE; EXON; HUMAN; POINT MUTATION; POLYMERASE CHAIN REACTION; RESTRICTION FRAGMENT LENGTH POLYMORPHISM;

EID: 0030828097     PISSN: 00411132     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1537-2995.1997.371098016441.x     Document Type: Article

References (8)

1. Redman CM, Marsh WL. The Kell blood group system and the McLeod phenotype. Semin Hematol 1993;30:209-18.
2. Redman CM, Lee S. Kell blood group system and the McLeod Syndrome. In: Cartron JP, Rouger P, eds. Molecular basis of human blood group antigens. Blood cell biochemistry, vol 6. New York: Plenum Press, 1995:227-42.
3. Lee S, Wu X, Reid M, et al. Molecular basis of the Kell (K1) phenotype. Blood 1995;85:912-6.
4. Lee S, Wu X, Son S, et al. Point mutations characterize KEL10, the KEL3, KEL4, and KEL21 alleles, and the KEL17 and KEL11 alleles. Transfusion 1996;36:490-4.
5. Lee S, Wu X, Reid M, Redman C. Molecular basis of the K:6,-7 [Js(a+b-)] phenotype in the Kell blood group system. Transfusion 1995;35:822-5.
6. Lee S, Zambas E, Green ED, Redman C. Organization of the gene encoding the human Kell blood group protein. Blood 1995;85:1364-70.
7. Lee S, Zambas ED, Marsh WL, Redman CM. Molecular cloning and primary structure of Kell blood group protein. Proc Natl Acad Sci U S A 1991;88:6353-7.
8. Jones J, Reid ME, Oyen R, et al. A novel common Kell antigen, TOU, and its spatial relationship to other Kell antigens. Vox Sang 1995;69:53-60.