Early Prenatal Diagnosis in Two Pregnancies at Risk for Glutaryl-CoA Dehydrogenase Deficiency
- 1 April 1989
- journal article
- case report
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 12 (2) , 280-282
- https://doi.org/10.1007/bf03335398
Abstract
No abstract availableKeywords
This publication has 5 references indexed in Scilit:
- ANTENATAL DIAGNOSIS OF GLUTARIC ACIDEMIA1980
- Studies on glutaryl-CoA dehydrogenase in leucocytes, fibroblasts and amniotic fluid cells. The normal enzyme and the mutant form in patients with glutaric aciduriaClinica Chimica Acta; International Journal of Clinical Chemistry, 1978
- Glutaric aciduria in progressive choreo‐athetosisClinical Genetics, 1978
- Intermittently Progressive Dyskinetic Syndrome in Glutaric AciduriaNeuropediatrics, 1977
- Glutaric aciduria; A “new” disorder of amino acid metabolismBiochemical Medicine, 1975