Author:
Berry Gerard T.,Walter John,Fridovich-Keil Judith L.
Publisher
Springer Berlin Heidelberg
Reference56 articles.
1. Berry G (2014) Classic Galactosemia and Clinical Variant Galactosemia. In: Pagon R, Adam M, Ardinger H et al. (eds) Gene Reviews, Seattle, Washington, University of Washington, Seattle
2. Berry G (2012) Galactosemia: when is it a newborn screening emergency? Mol Genet Metab 106:7–11
3. Fridovich-Keil J, Walter J (2008) Galactosemia. In: Valle D, Beaudet A, Vogelstein B (eds) The Online Metabolic & Molecular Bases of Inherited Disease. McGraw Hill;
http://www.ommbid.com/
4. Berry GT, Moate PJ, Reynolds RA et al. (2004) The rate of de novo galactose synthesis in patients with galactose-1-phosphate uridyltransferase deficiency. Mol Genet Metab 81:22–30
5. Schadewaldt P, Kamalanathan L, Hammen HW, Wendel U (2004) Age dependence of endogenous galactose formation in Q188R homozygous galactosemic patients. Mol Genet Metab 81:31–44
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