Succoio, M., Sacchettini, R., Rossi, A., Parenti, G., & Ruoppolo, M. 2022. Galactosemia: Biochemistry, Molecular Genetics, Newborn Screening, and Treatment. Biomolecules, 12(7), 968. https://doi.org/10.3390/biom12070968
Kikuchi, A.; Wada, Y.; Ohura, T.; Kure, S. 2021. The Discovery of GALM Deficiency (Type IV Galactosemia) and Newborn Screening System for Galactosemia in Japan. Julkaistu lehdessä Neonatal Screen. DOI: https://doi.org/10.3390/ijns7040068
Chhay, J.S.; Vargas, C.A.; McCorvie, T.J.; Fridovich-Keil, J.L.; Timson, D.J. 2008. Analysis of UDP-galactose 4’-epimerase mutations associated with the intermediate form of type III galactosaemia. Julkaistu lehdessä Journal of inherited metabolic disease. DOI: https://doi.org/10.1007/s10545-007-0790-9
Fridovich-Keil, J.L. (2006), Galactosemia: The good, the bad, and the unknown. J. Cell. Physiol., 209: 701-705. https://doi.org/10.1002/jcp.20820
nih.gov
ncbi.nlm.nih.gov
Berry, G.T. 2000. Classic Galactosemia and Clinical Variant Galactosemia. Julkaistu lehdessöIn Gene Reviews. Saatavilla ONLINE, katsottu 5.11.2022. https://www.ncbi.nlm.nih.gov/books/NBK1518/
