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D-GLYCERIC ACIDURIA

An autosomal recessive genetic disorder caused by mutations in the GLYCTK gene, encoding glycerate kinase. The condition is characterized by… 
National Institutes of Health

Papers overview

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1993
1993
Hyperoxaluria type II (McKusick 260000) is a very rare metabolic disorder characterized by renal disease and excessive excretion… 
1988
1988
L-Glyceric aciduria (primary hyperoxaluria type 2; McKusick 26000) is a rare inherited disorder characterized in man by recurrent… 
Review
1988
Review
1988
Primary hyperoxaluria is an uncommon autosomal recessive disorder. The clinical features consist of nephrocalcinosis, recurrent… 
1984
1984
In a mentally retarded boy, who excreted elevated amounts of glycine,d-glyceric acid and acylglycines and whose cells exhibited… 
1978
1978
Hydroxypyruvate and glycolate inhibited the oxidation of [U-14C]glyoxylate to [14C]oxalate in isolated perfused rat liver, but… 
1977
1977
The patient, a boy, was born of healthy parents after a normal pregnancy. Birth was uncomplicated; birth weight 3350 g. In the… 
1966
1966
The biological importance of glycerol and glyceric acid is well known; as a consequence, it is very useful to have methods for… 
1937
1937
IT has been found1 that ferricyanide (10−2 mol./litre) stops œrobic glycolysis of mammalian tumour cells, but it does not affect…