Hereditary Fructose Intolerance

Author:

Cox Timothy M.

Publisher

Elsevier

Reference147 articles.

1. Diverse mutations in the aldolase B gene that underlie the prevalence of hereditary fructose intolerance. Independent segregation of four mutant alleles in ten affected members of a large kindred;Ali;Am. J. Hum. Genet.,1995

2. A newly-identified aldolase B splicing mutation (G-→C, 5′ intron 5) in hereditary fructose intolerance from New Zealand;Ali;Hum. Mutat.,1996

3. Hereditary fructose intolerance;Ali;J. Med. Genet.,1998

4. DNA diagnosis of fatal fructose intolerance from archival tissue;Ali;Q. J. Med.,1993

5. Identification of a novel mutation (Leu 256→Pro) in the human aldolase B gene associated with hereditary fructose intolerance;Ali;Hum. Mol. Genet.,1994

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1. Impaired Carbohydrate Metabolism in Metabolic Disorders;Emerging Contaminants and Associated Treatment Technologies;2020-08-05

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