Author:
Pena Loren,Franks Jill,Chapman Kimberly A.,Gropman Andrea,Ah Mew Nicholas,Chakrapani Anupam,Island Eddie,MacLeod Erin,Matern Dietrich,Smith Brittany,Stagni Kathy,Sutton V. Reid,Ueda Keiko,Urv Tiina,Venditti Charles,Enns Gregory M.,Summar Marshall L.
Subject
Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism
Reference60 articles.
1. Idiopathic hyperglycinemia and hyperglycinuria: a new disorder of amino acid metabolism I;Childs;Pediatrics,1961
2. Idiopathic hyperglycinemia: a new disorder of amino acid metabolism. II. The concentrations of other amino acids in the plasma and their modification by the administration of leucine;Nyhan;Pediatrics,1961
3. Defective propionate carboxylation in ketotic hyperglycinaemia;Hsia;Lancet,1969
4. Localisation of enzymic defect in propionicacidaemia;Gompertz;Lancet,1970
5. Inherited propionyl-Coa carboxylase deficiency in “ketotic hyperglycinemia”;Hsia;J. Clin. Invest.,1971
Cited by
116 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献