Published 1989
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Dystonia and Infantile Glutaric Acidemia
- Creators
- Millichap, J. Gordon
Abstract
Glutaric acidemia, an autosomal recessively inherited disease caused by deficiency of glutaryl-CoA dehydrogenase, was manifested by acute dystonia in 3 infants reported from the Children's Hospital of Pittsburgh, Pennsylvania.
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- Other
- PNB-3-04
- Created
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1989When the item was originally created.