Point mutations causing the McLeod phenotype.

Transfusion

Volumn 42, Issue 3, 2002, Pages 287-293

  Russo, David C W ^a   Lee, Soohee ^a   Reid, Marion E ^a   Redman, Colvin M ^a  

^a NEW YORK BLOOD CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ACANTHOCYTOSIS; ANIMAL; ARTICLE; BLOOD GROUP KELL SYSTEM; CELL STRAIN COS1; CODON; DNA SEQUENCE; ERYTHROCYTE; EXON; GENETIC TRANSFECTION; GENETICS; GENOTYPE; HUMAN; IMMUNOLOGY; INTRON; MALE; NEUROMUSCULAR DISEASE; PHENOTYPE; POINT MUTATION; POLYACRYLAMIDE GEL ELECTROPHORESIS; POLYMERASE CHAIN REACTION; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; RNA SPLICING; SYNDROME; WESTERN BLOTTING; X CHROMOSOME;

ACANTHOCYTES; ANIMALS; BLOTTING, WESTERN; CODON; COS CELLS; DNA; ELECTROPHORESIS, POLYACRYLAMIDE GEL; ERYTHROCYTES; EXONS; GENOTYPE; HUMANS; INTRONS; KELL BLOOD-GROUP SYSTEM; MALE; NEUROMUSCULAR DISEASES; PHENOTYPE; POINT MUTATION; POLYMERASE CHAIN REACTION; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; RNA SPLICING; SEQUENCE ANALYSIS, DNA; SYNDROME; TRANSFECTION; X CHROMOSOME;

EID: 0036519357     PISSN: 00411132     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1537-2995.2002.00049.x     Document Type: Article

References (0)