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LANCET, ISSN 0140-6736, 01/2008, Volume 371, Issue 9606, pp. 64 - 74
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common human enzyme defect, being present in more than 400 million people worldwide. The global... 
HEMOLYTIC-ANEMIA | MOLECULAR CHARACTERIZATION | MALARIA-G-6-PD HYPOTHESIS | SEVERE NEONATAL HYPERBILIRUBINEMIA | SEQUENCE-ANALYSIS | MEDICINE, GENERAL & INTERNAL | G6PD DEFICIENCY | PLASMODIUM-FALCIPARUM | PYRUVATE-KINASE DEFICIENCY | RED-CELLS | GLUCOSE-6-PHOSPHATE-DEHYDROGENASE DEFICIENCY
Journal Article
Journal Article
G6PD deficiency in Vataliya prajapati community settled in Surat, 12/2005
BACKGROUND: A Study on Vataliya Prajapati was published earlier but heterozygous females were not identified. AIMS: To compare incidence of glucose-6-phosphate... 
G6PD deficiency, Vataliya Prajapati, G6PD enzyme activity, Hemolytic crisis, Chronic hemolytic anemia
Journal
Gene, ISSN 0378-1119, 10/2019, Volume 715, p. 144027
To explore the clinical and molecular characteristics of a Chinese Zhuang minority patient with leukocyte adhesion deficiency type-1 (LAD-1) and... 
Primary immunodeficiency disease | Rare genetic disorder | G6PD | Ethnic minority group | ITGB2 | MOLECULAR CHARACTERIZATION | MIGRATION | G6PD DEFICIENCY | LFA-1 | INTEGRIN | GENETICS & HEREDITY | EXPRESSION | SUBUNIT
Journal Article
Journal Article