Author:
Roe Thomas F.,Ng Won G.,Smit Peter G. A.
Publisher
Springer Berlin Heidelberg
Reference10 articles.
1. Gitzelmann R (2000) Disorders of galactose metabolism. In: Inborn metabolic diseases, Fernandes J, Saudubray J-M, van den Berghe G (eds). Springer-Verlag Berlin Heidelberg New York, 3rd edition: 201–209.
2. Shin YS, Zschocke J, Das AM, Podskarbi T (1999) Molecular and biochemical basis for variants and deficiency forms of galactose-1-phosphate uridyltransferase. J Inherit Metab Dis 22:327–329.
3. Clayton PE (2000) Recommendations for the management of galactosemia. Arch Dis Child 82:336.
4. Van den Berghe G (2000) Disorders of fructose metabolism. In: Inborn metabolic diseases, Fernandes J, Saudubray J-M, van den Berghe G (eds). Springer-Verlag Berlin Heidelberg New York, 3rd edition: 110–116.
5. Ali M, Rellos P, Cox TM (1998) Hereditary fructose intolerance. J Med Genet 35:353–365.