Detection of inborn errors of metabolism
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1974.tb00634.x/fullpdf
Reference18 articles.
1. The oxidation of glycine and propionic acid in propionic acidemia with ketotic hyperglycinemia;Ando;Pediat. Res.,1972a
2. 3-Hydroxypropionate: Significance of (β-oxidation of propionate in patients with propionic acidemia and methylmalonic acidemia;Ando;Proc. not. Acad. Sci. (Wash.),1972b
3. Homocystinuria with methylmelonic aciduria: two cases in a sibship;Goodman;Biochem. Med.,1970
4. Detection of inborn errors of metabolism: Galactosemia;Hill;Science,1973
5. Propionic acidemia, a new inborn error of metabolism;Hommes;Pediat. Res.,1968
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1. Import of TAT-Conjugated Propionyl Coenzyme A Carboxylase Using Models of Propionic Acidemia;Molecular and Cellular Biology;2018-03-15
2. A simple, rapid method for prenatal detection of defects in propionate metabolism;Clinical Genetics;2008-04-23
3. Detection of inborn errors of metabolism. IV. Galactokinase deficiency;Clinical Genetics;2008-04-23
4. Detection of inborn errors of metabolism;Clinical Genetics;2008-04-23
5. Increased excretion of propan-1,3-diol and 3-hydroxypropionic acid apparently caused by abnormal bacterial metabolism in the gut;Clinica Chimica Acta;1987-11
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