[Congenital deficiency in glucose-6-phosphate dehydrogenase. Slow variant found in a Spanish family. Relation with the variant Gd(minus) "Seattle" (author's transl)]. 1974

J L Vives Corrons, and A Carrera, and A Kahn, and J Triginer, and C Rozmán

UI MeSH Term Description Entries
D008297 Male Males
D002648 Child A person 6 to 12 years of age. An individual 2 to 5 years old is CHILD, PRESCHOOL. Children
D004912 Erythrocytes Red blood cells. Mature erythrocytes are non-nucleated, biconcave disks containing HEMOGLOBIN whose function is to transport OXYGEN. Blood Cells, Red,Blood Corpuscles, Red,Red Blood Cells,Red Blood Corpuscles,Blood Cell, Red,Blood Corpuscle, Red,Erythrocyte,Red Blood Cell,Red Blood Corpuscle
D005838 Genotype The genetic constitution of the individual, comprising the ALLELES present at each GENETIC LOCUS. Genogroup,Genogroups,Genotypes
D005955 Glucosephosphate Dehydrogenase Deficiency A disease-producing enzyme deficiency subject to many variants, some of which cause a deficiency of GLUCOSE-6-PHOSPHATE DEHYDROGENASE activity in erythrocytes, leading to hemolytic anemia. Deficiency of Glucose-6-Phosphate Dehydrogenase,Deficiency, GPD,Deficiency, Glucosephosphate Dehydrogenase,G6PD Deficiency,GPD Deficiency,Glucose 6 Phosphate Dehydrogenase Deficiency,Glucose-6-Phosphate Dehydrogenase Deficiency,Glucosephosphate Dehydrogenase Deficiencies,Hemolytic Anemia Due to G6PD Deficiency,Deficiencies, G6PD,Deficiencies, GPD,Deficiencies, Glucose-6-Phosphate Dehydrogenase,Deficiencies, Glucosephosphate Dehydrogenase,Deficiency of Glucose 6 Phosphate Dehydrogenase,Deficiency, G6PD,Deficiency, Glucose-6-Phosphate Dehydrogenase,Dehydrogenase Deficiencies, Glucose-6-Phosphate,Dehydrogenase Deficiencies, Glucosephosphate,Dehydrogenase Deficiency, Glucose-6-Phosphate,Dehydrogenase Deficiency, Glucosephosphate,G6PD Deficiencies,GPD Deficiencies,Glucose-6-Phosphate Dehydrogenase Deficiencies
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man

Related Publications

J L Vives Corrons, and A Carrera, and A Kahn, and J Triginer, and C Rozmán
July 1974, Biomedicine / [publiee pour l'A.A.I.C.I.G.],
J L Vives Corrons, and A Carrera, and A Kahn, and J Triginer, and C Rozmán
January 1973, Nouvelle revue francaise d'hematologie,
J L Vives Corrons, and A Carrera, and A Kahn, and J Triginer, and C Rozmán
January 1972, Enzyme,
J L Vives Corrons, and A Carrera, and A Kahn, and J Triginer, and C Rozmán
June 1978, La Nouvelle presse medicale,
J L Vives Corrons, and A Carrera, and A Kahn, and J Triginer, and C Rozmán
January 1984, Acta haematologica,
J L Vives Corrons, and A Carrera, and A Kahn, and J Triginer, and C Rozmán
January 1987, Pediatriia,
J L Vives Corrons, and A Carrera, and A Kahn, and J Triginer, and C Rozmán
November 1965, The Journal of laboratory and clinical medicine,
J L Vives Corrons, and A Carrera, and A Kahn, and J Triginer, and C Rozmán
January 1970, Nouvelle revue francaise d'hematologie,
J L Vives Corrons, and A Carrera, and A Kahn, and J Triginer, and C Rozmán
January 1980, Human genetics,
Copied contents to your clipboard!