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Mudd SH, Cerone R, Schiaffino MC, Fantasia AR, Minniti G, Caruso U, Lorini R, Watkins D, Matiaszuk N, Rosenblatt DS, Schwahn B, Rozen R, LeGros L, Kotb M, Capdevila A, Luka Z, Finkelstein JD, Tangerman A, Stabler SP, Allen RH, Wagner C. Glycine N‐methyltransferase deficiency: A novel inborn error causing persistent isolated hypermethioninaemia. J of Inher Metab Disea. 2001 Jul;24(4):448–64. doi: 10.1023/a:1010577512912. |