Transient hyperammonaemia.

Abstract

Journal of Inherited Metabolic DiseaseVolume 10, Issue 3 p. 269-269 Case Report Transient hyperammonaemia D. J. Harris, D. J. Harris Sections of Genetics and Neurology, The Children's Mercy Hospital, The University of Missouri, Kansas City, MO, 64108 USASearch for more papers by this authorC. Siegel, C. Siegel Sections of Genetics and Neurology, The Children's Mercy Hospital, The University of Missouri, Kansas City, MO, 64108 USASearch for more papers by this authorR. E. Baska, R. E. Baska Sections of Genetics and Neurology, The Children's Mercy Hospital, The University of Missouri, Kansas City, MO, 64108 USASearch for more papers by this author D. J. Harris, D. J. Harris Sections of Genetics and Neurology, The Children's Mercy Hospital, The University of Missouri, Kansas City, MO, 64108 USASearch for more papers by this authorC. Siegel, C. Siegel Sections of Genetics and Neurology, The Children's Mercy Hospital, The University of Missouri, Kansas City, MO, 64108 USASearch for more papers by this authorR. E. Baska, R. E. Baska Sections of Genetics and Neurology, The Children's Mercy Hospital, The University of Missouri, Kansas City, MO, 64108 USASearch for more papers by this author First published: 01 September 1987 https://doi.org/10.1007/BF01800074 The PCC assay was performed by Dr Barry Wolf, University of Virginia. AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinkedInRedditWechat No abstract is available for this article. Volume10, Issue3September 1987Pages 269-269 RelatedInformation