Profound Biotinidase Deficiency: A Rare but Treatable Inborn Error of Metabolism in a Neonate with Recurrent Seizures
| Main Authors: | , , , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Korean Child Neurology Society
2024-01-01
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| Series: | Annals of Child Neurology |
| Online Access: | http://annchildneurol.org/upload/pdf/acn-2023-00192.pdf |