Bouteldja, Timson: "The biochemical basis of hereditary fructose intolerance." in: Journal of inherited metabolic disease, Vol. 33, Issue 2, pp. 105-12, 2010 (PubMed).
Coffee, Yerkes, Ewen et al.: "Increased prevalence of mutant null alleles that cause hereditary fructose intolerance in the American population." in: Journal of inherited metabolic disease, Vol. 33, Issue 1, pp. 33-42, 2010 (PubMed).
Segat, Milanese, Pirulli et al.: "Secreted protein acidic and rich in cysteine (SPARC) gene polymorphism association with hepatocellular carcinoma in Italian patients." in: Journal of gastroenterology and hepatology, Vol. 24, Issue 12, pp. 1840-6, 2009 (PubMed).
Eriksson, Flach, Lindgren et al.: "Five mucosal transcripts of interest in ulcerative colitis identified by quantitative real-time PCR: a prospective study." in: BMC gastroenterology, Vol. 8, pp. 34, 2008 (PubMed).
Davit-Spraul, Costa, Zater et al.: "Hereditary fructose intolerance: frequency and spectrum mutations of the aldolase B gene in a large patients cohort from France--identification of eight new mutations." in: Molecular genetics and metabolism, Vol. 94, Issue 4, pp. 443-7, 2008 (PubMed).