Studies on glutaryl-CoA dehydrogenase in leucocytes, fibroblasts and amniotic fluid cells. The normal enzyme and the mutant form in patients with glutaric aciduria
Author:
Publisher
Elsevier BV
Subject
Biochemistry, medical,Clinical Biochemistry,Biochemistry,General Medicine
Reference14 articles.
1. Glutaric aciduria; A “new” disorder of amino acid metabolism
2. Glutaric aciduria: Inherited deficiency of glutaryl-CoA dehydrogenase activity
3. Glutaric aciduria: Biochemical and morphologic considerations
4. Glutaric aciduria: Clinical and laboratory findings in two brothers
5. Glutaric aciduria in progressive choreo-athetosis
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