An alanine-to-threonine substitution in protein 4.2 cDNA is associated with a Japanese form of hereditary hemolytic anemia (protein 4.2^NIPPON)

Medicine & Life Sciences

• Congenital Hemolytic Anemia 100%
• Threonine 69%
• Alanine 63%
• Complementary DNA 50%
• Protein Deficiency 32%
• Proteins 22%
• Mutation 17%
• Chromosomes 14%
• Haemolytic Anaemia 14%
• Membrane Proteins 10%
• Hereditary Spherocytosis 9%
• RNA Isoforms 8%
• Reticulocytes 7%
• Membranes 7%
• Polymerase Chain Reaction 7%
• DNA-Directed RNA Polymerases 6%
• Sodium Dodecyl Sulfate 6%
• Codon 6%
• Point Mutation 6%
• Polyacrylamide Gel Electrophoresis 5%
• Reverse Transcription 5%
• Exons 5%
• Erythrocytes 4%
• Parents 4%
• Alleles 4%
• DNA 3%

Chemical Compounds

• Haemolytic 71%
• Complementary DNA 64%
• Substitution Reaction 39%
• Protein 25%
• Mutation 19%
• Threonine 4%
• Chain Reaction 3%
• Alanine 3%