Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitlePersistent hypocitrullinaemia as a marker for mtDNA NARP T 8993 G mutation?AuthorsRabier, D.; Diry, C.; Rotig, A.; Rustin, P.; Heron, B.; Bardet, J.; Parvy, P.; Ponsot, G.; Marsac, C.; Saudubray, J.; Munnich, A.; Kamoun, P.PublicationJournal of Inherited Metabolic Disease, 1998, Vol 21, Issue 3, p216ISSN0141-8955Publication typeArticleDOI10.1023/A:1005391300203