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Ornithine carbamoyltransferase deficiency: unusual clinical findings and novel mutation

V E Shih1, A P Safran, A H Ropper

  • 1Neurology Service, Massachusetts General Hospital, Boston 02129, USA. vshih@partners.org

Journal of Inherited Metabolic Disease
|July 10, 1999
PubMed
Abstract

No abstract available in PubMed .

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