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GlycineN-methyltransferase deficiency: A novel inborn error causing persistent isolated hypermethioninaemia

✍ Scribed by S.H. Mudd; R. Cerone; M.C. Schiaffino; A.R. Fantasia; G. Minniti; U. Caruso; R. Lorini; D. Watkins; N. Matiaszuk; D.S. Rosenblatt; B. Schwahn; R. Rozen; L. LeGros; M. Kotb; A. Capdevila; Z. Luka; J.D. Finkelstein; A. Tangerman; S.P. Stabler; R.H. Allen; C. Wagner

Book ID: 110292234
Publisher: Springer
Year: 2001
Tongue: English
Weight: 138 KB
Volume: 24
Category: Article
ISSN: 0141-8955
DOI: 10.1023/a:1010577512912

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