Clumsiness, confusion, coma, and valproate
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference5 articles.
1. Structure of the human ornithine transcarbamylase gene;Hata;J Biochem,1988
2. Identification of “private” mutations in patients with omithine transcarbamylase deficiency;Tuchman;J Inher Metab Dis,1997
3. Urea cycle enzymes;Brusilow,1995
4. Valproate toxicity and ornithine carbamoyltransferase deficiency;Kay;Lancet,1986
5. Heterozygote ornithine transcarbamylase deficiency presenting as symptomatic hyperammonaemia during initiation of valproate therapy;Honeycutt;Neurol,1992
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