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

Keyphrases

• Complementary DNA (cDNA) 100%
• Threonine 100%
• Protein 4.2 100%
• Hereditary Hemolytic Anemia 100%
• Hemolytic Anemia 12%
• RBC Membrane 12%
• Subclone 6%
• Clinical Presentation 6%
• Genomic DNA (gDNA) 6%
• Sodium Dodecyl Sulfate Polyacrylamide Gel Electrophoresis (SDS-PAGE) 6%
• Reticulocytes 6%
• Doublet 6%
• Erythrocytes 6%
• Membrane Protein 6%
• Codon 6%
• Reverse Transcription 6%
• Polymerase Chain Reaction 6%
• Heterozygosity 6%
• RNA Splicing 6%
• Splice Isoforms 6%
• Alternatively Spliced Exons 6%
• Rapid Screening 6%
• Restriction Sites 6%
• Allele-specific Hybridization 6%
• Hereditary Spherocytosis 6%
• Japanese Learners 6%
• Spherocytosis 6%
• Single-point mutation 6%
• Polymerase Chain Reaction Amplification 6%
• Variant Form 6%

Biochemistry, Genetics and Molecular Biology

• Protein 4.2 100%
• Threonine 100%
• Alanine 100%
• Deficiency 25%
• Chromosome 18%
• Spherocytosis 12%
• Polymerase Chain Reaction 12%
• Exon 6%
• Isoform 6%
• RNA 6%
• Allele 6%
• Polyacrylamide Gel Electrophoresis 6%
• Membrane Protein 6%
• Codon 6%
• Reverse Transcription 6%
• Point Mutation 6%
• Heterozygosity 6%
• RNA Splicing 6%
• Restriction Site 6%
• Subcloning 6%
• Genomics 6%
• Reticulocyte 6%