Results
1 -
10 of
13New Cases of DHTKD1 Mutations in Patients with 2-Ketoadipic Aciduria, JIMD Reports, Volume 25 Disorders of Ornithine, Lysine and Tryptophan, Physicianu2019s Guide to the Laboratory Diagnosis of Metabolic Diseases Cerebral Organic Acid Disorders and Other Disorders of Lysine Catabolism, Inborn Metabolic Diseases NADH-dependent lactate dehydrogenase from Alcaligenes eutrophus H16 reduces 2-oxoadipate to 2-hydroxyadipate, Biotechnology and Bioprocess Engineering Abnormal ??-aminoadipic acid excretion in a newborn with a defect in platelet aggregation and antenatal cerebral haemorrhage, Journal of Inherited Metabolic Disease ??-Aminoadipic and ??-Ketoadipic Aciduria: Detection of a New Case by a Screening Program using Two-dimensional Thin Layer Chromatography of Amino Acids, Inherited Disorders of Vitamins and Cofactors Recurrent, familial Reye-like syndrome with a new complex amino and organic aciduria, European Journal of Pediatrics Biochemical and clinical studies of a new case of ??-aminoadipic aciduria, Journal of Inherited Metabolic Disease Lysine inhibition of Saccharomyces cerevisiae: role of repressible L-lysine ??-aminotransferase, World Journal of Microbiology & Biotechnology ??-Aminoadipic aciduria, a non-deleterious inborn metabolic defect, Humangenetik