Skip to search formSkip to main contentSkip to account menu

Deficiency of glucose-6-phosphate dehydrogenase

Known as: Deficiency, G6PD, Deficiencies, GPD, Deficiency of Glucose 6 Phosphate Dehydrogenase 
An X-linked recessive inherited disorder caused by mutations in the G6PD gene. It is characterized by the absence or presence of very low levels of… 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
1986
Highly Cited
1986
Glycerol dehydrogenase (GDH, EC 1.1.1.6, from Enterobacter aerogenes or Cellulomonas sp.) catalyzes the interconversion of… 
Highly Cited
1976
Highly Cited
1976
Human fibroblasts containing a translocation between the X chromosome and chromosome 15 were fused with the 6-thioguanine… 
Highly Cited
1974
Highly Cited
1974
Abstract— Ovariectomized female rats were treated daily with oestradiol‐17β benzoate for intervals up to one week and enzyme… 
Highly Cited
1972
Highly Cited
1972
Abstract The extremely young red-cell population in sickle-cell anemia invariably results in increased G-6-PD activity. This… 
Highly Cited
1962
Highly Cited
1962
Glucose-6-phosphate dehydrogenase (G-6-PD) deficiency is an inborn error of metabolism. It leads to reduction of red cell…