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Nijland, Hartog, Wevers et al.: "Galactose-1-phosphate uridyl transferase deficiency is not associated with Müllerian aplasia in Dutch patients." in: Journal of pediatric and adolescent gynecology, Vol. 22, Issue 4, pp. 229-31, 2009 (PubMed).
Facchiano, Marabotti: "Analysis of galactosemia-linked mutations of GALT enzyme using a computational biology approach." in: Protein engineering, design & selection : PEDS, Vol. 23, Issue 2, pp. 103-13, 2010 (PubMed).
Ounap, Joost, Temberg et al.: "Classical galactosemia in Estonia: selective neonatal screening, incidence, and genotype/phenotype data of diagnosed patients." in: Journal of inherited metabolic disease, Vol. 33, Issue 2, pp. 175-6, 2010 (PubMed).
Davila, Froeling, Tan et al.: "New genetic associations detected in a host response study to hepatitis B vaccine." in: Genes and immunity, Vol. 11, Issue 3, pp. 232-8, 2010 (PubMed).
Ko, Chang, Song et al.: "Molecular and biochemical characterization of the GALT gene in Korean patients with galactose-1-phosphate uridyltransferase deficiency." in: Clinica chimica acta; international journal of clinical chemistry, Vol. 411, Issue 19-20, pp. 1506-10, 2010 (PubMed).