Malonyl coenzyme A decarboxylase deficiency.

Author:

MacPhee G B,Logan R W,Mitchell J S,Howells D W,Tsotsis E,Thorburn D R

Publisher

BMJ

Subject

Pediatrics, Perinatology and Child Health

Reference8 articles.

1. Malonyl CoA decarboxylase deficiency. J7 Inherited Metab;Brown, G.K.; Scholem, R.D.; Bankier, A.; Danks, D.M.;Dis,1984

2. Malonyl CoA decarboxylase deficiency - a further case with an unusual pattern of organic acids in the urine. Abstracts of the 22nd Annual Symposium of the Society for the Study ofInborn Errors ofMetabolism;Danks, D.M.; Brown, G.K.; Haan, E.A.; Hunt, S.; Scholem, R.;Newcastle-upon-Tyne

3. Malonyl coenzyme A decarboxylase deficiency. Clinical and biochemical findings in a second child with a more severe enzyme defect;Haan, E.A.; Scholem, R.D.; Croll, H.B.; Brown, G.K.;Eur Pediatr,1986

4. Gaschromatographic method of analysis for urinary organic acids. I. Retention indices of 155 metabolically important compounds;Tanaka, K.; Hine, D.G.; West-Dull, A.; Lynn, T.B.;Clin Chem,1980

5. Gaschromatographic method of analysis for urinary organic acids. II. Description of the procedure, and its application to the diagnosis of patients with organic acidurias;Tanaka, K.; West-Dull, A.; Hine, D.G.; Lynn, T.B.; Lowe, T.;Clin Chem,1980

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