Orotic Aciduria Fibroblasts Express a Labile Form of UMP Synthase
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference31 articles.
1. Uridine-responsive hypogammaglobulinemia and congenital heart disease in a patient with hereditary orotic aciduria
2. Hereditary Orotic Aciduria and Megaloblastic Anaemia: A Second Case, with Response to Uridine
3. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding
4. Amino Acid Metabolism in Mammalian Cell Cultures
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1. Hereditary orotic aciduria (HOA): A novel uridine-5-monophosphate synthase (UMPS) mutation;Molecular Genetics and Metabolism Reports;2021-03
2. Disorders of Purine and Pyrimidine Metabolism;Inborn Metabolic Diseases;2012
3. Disorders of Purine and Pyrimidine Metabolism;Inborn Metabolic Diseases;2006
4. Diagnostic value of urinary orotic acid levels: applicable separation methods;Journal of Chromatography B;2002-12
5. Disorders of Purine and Pyrimidine Metabolism;Inborn Metabolic Diseases;2000
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