Author:
Valadares Eugênia Ribeiro,Cruz Ana Facury da,Adelino Talita Emile Ribeiro,Kanufre Viviane de Cássia,Ribeiro Maria do Carmo,Penido Maria Goretti Moreira Guimarães,Peret Filho Luciano Amedee,Valadares Laís Maria Santos Valadares e
Subject
Endocrinology,Genetics,Molecular Biology
Reference34 articles.
1. Steinman B, Gitzelmann R, van den Berghe G. Disorders of fructose metabolism. In: Scriver CR, Beaudet AL, Valle D, Sly WS, editors. The Metabolic and Molecular Bases of Inherited Disease. New York: McGraw-Hill; 2001;1489–1520.
2. The biochemical basis of hereditary fructose intolerance;Bouteldja;J Inherit Metab Dis,2010
3. Molecular basis of hereditary fructose intolerance: mutations and polymorphisms in human aldolase B gene;Tolan;Hum Mutat,1995
4. Neonatal screening for hereditary fructose intolerance: frequency of the most common mutant aldolase B allele (A149P) in the British population;James;J Med Genet,1996
5. Integration of PCR sequencing analysis with multiplex ligation-dependent probe amplification for diagnosis of hereditary fructose intolerance;Ferri;JIMD Rep,2012
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