Back to matchesWe found a matchYour institution may have rights to this item. Sign in to continue.TitleGlycine N -methyltransferase deficiency: A novel inborn error causing persistent isolated hypermethioninaemia.AuthorsMudd, S.; Cerone, R.; Schiaffino, M.; Fantasia, A.; Minniti, G.; Caruso, U.; Lorini, R.; Watkins, D.; Matiaszuk, N.; Rosenblatt, D.; Schwahn, B.; Rozen, R.; LeGros, L.; Kotb, M.; Capdevila, A.; Luka, Z.; Finkelstein, J.; Tangerman, A.; Stabler, S.; Allen, R.PublicationJournal of Inherited Metabolic Disease, 2001, Vol 24, Issue 4, p448ISSN0141-8955Publication typeArticleDOI10.1023/A:1010577512912