Guanidinoacetate methyltransferase deficiency: First steps to newborn screening for a treatable neurometabolic disease

S. Mercimek-Mahmutoglu, G. Sinclair, S. J.M. van Dooren, W. Kanhai, P. Ashcraft, O. J. Michel, J. Nelson, O. T. Betsalel, L. Sweetman, C. Jakobs, G. S. Salomons

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