Publication | Closed Access
l-arginine:glycine amidinotransferase (AGAT) deficiency: Clinical presentation and response to treatment in two patients with a novel mutation
52
Citations
17
References
2010
Year
Novel MutationGenetic DisorderGeneticsInherited Metabolic DiseaseGlycine AmidinotransferaseClinical PresentationPathologyMedicineLysosomal Storage Disease
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