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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| Hlavní autor: | |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Pediatric Neurology Briefs Publishers
1989-01-01
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| Edice: | Pediatric Neurology Briefs |
| Témata: | |
| On-line přístup: | https://www.pediatricneurologybriefs.com/articles/3434 |
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