Combined iminoglycinuria and cystine- and dibasic aminoaciduria in patients with propionic acidaemia and 3-methylcrotonylglycinuria
- 1 December 1980
- journal article
- Published by Springer Nature in Journal of Inherited Metabolic Disease
- Vol. 3 (1) , 85-86
- https://doi.org/10.1007/bf02312533
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
- Age Related Reference Values for Urinary Free Amino Acids: A Simple Method of Evaluationcclm, 1979
- The variability of metabolite excretion in propionicacidaemiaClinica Chimica Acta; International Journal of Clinical Chemistry, 1978
- COMBINED CARBOXYLASE DEFECT: BIOTIN-RESPONSIVENESS IN CULTURED FIBROBLASTSThe Lancet, 1976
- Rapid Screening Methods for the Detection of Inherited and Acquired AminoacidopathiesPublished by Elsevier ,1971
- Inherited propionyl-CoA carboxylase deficiency in “ketotic hyperglycinemia”Journal of Clinical Investigation, 1971
- The excretion of amino acids by cystinuric patients and their relativesAnnals of Human Genetics, 1969