The Molecular Basis of a Case of γ-Glutamylcysteine Synthetase Deficiency - Beutler, Ernest; Gelbart, Terri; Kondo, Takahito; Matsunaga, Alison T. (Blood, 1999)
Keywords: Adolescent; Amino Acid Metabolism, Inborn Errors - blood; Amino Acid Metabolism, Inborn Errors - genetics; Amino Acid Sequence; Amino Acid Substitution; Anemia, Hemolytic - blood; Anemia, Hemolytic - enzymology; Anemia, Hemolytic - genetics; Anemias. Hemoglobinopathies; Animals; Base Sequence; Biological and medical sciences; Catalytic Domain - genetics; Codon - genetics; Consanguinity; Diseases of red blood cells; DNA Primers; DNA, Complementary - genetics; Erythrocytes - enzymology; Female; Genes; Glutamate-Cysteine Ligase - deficiency; Glutamate-Cysteine Ligase - genetics; Glutathione - deficiency; Hematologic and hematopoietic diseases; Homozygote; Humans; Learning Disabilities - blood; Learning Disabilities - enzymology; Learning Disabilities - genetics; Lymphocytes - chemistry; Medical sciences; Mice; Molecular Sequence Data; Point Mutation; Rats; Recombinant Fusion Proteins - metabolism; Species Specificity; Transfection; Human; Enzyme; Family study; Deficiency; Red blood cell; Metabolic diseases; Hemopathy; Enzymopathy; Genetic disease; Case study; Hemolytic anemia; Gene; Genetics; Mutation; Glutathione; Polymorphism