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

✍ Scribed by 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


Book ID
118507160
Publisher
Elsevier Science
Year
2012
Tongue
English
Weight
318 KB
Volume
107
Category
Article
ISSN
1096-7192

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