Reversible Valproate Hepatotoxicity and Associated Mitochondrial Disease
A 2-year-old boy with seizures complicated by reversible valproate-induced hepatic failure was subsequently found to have mitochondrial polymerase g gene (POLG1) mutations typical of Alpers-Huttenlocher disease, in a study at Newcastle University, UK.
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Format: | Book |
Published: |
Pediatric Neurology Briefs Publishers,
2008-02-01T00:00:00Z.
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Connect to this object online.3rd Floor Main Library
Call Number: |
A1234.567 |
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Copy 1 | Available |