Dystonia and Infantile Glutaric Acidemia
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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| Format: | Book |
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Pediatric Neurology Briefs Publishers,
1989-01-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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