The genetic consequences of our sweet tooth

Author:

Cox Timothy M.

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics,Molecular Biology

Reference38 articles.

1. Cross, N. C. P., Tolan, D. R. & Cox, T. M. Catalytic deficiency of human aldolase B in hereditary fructose intolerance caused by a common missense mutation. Cell 53, 881–885 (1988).

2. Steinmann, B., Gitzelmann, R. & Van den Berghe, G. in The Metabolic and Molecular Bases of Inherited Disease 8th edn (eds Scriver, C. R., Beaudet, A. L., Sly, W. S. & Valle, D.) 1489–1520 (McGraw–Hill, New York, 2001).

3. Chambers, R. A. & Pratt, R. T. C. Idiosyncrasy to fructose. Lancet 2, 340 (1956).

4. Ali, M., Rellos, P. & Cox, T. M. Hereditary fructose intolerance. J. Med. Genet. 35, 353–365 (1998).

5. Brooks, C. C. & Tolan, D. R. Association of the widespread A149P hereditary fructose intolerance mutation with newly-identified sequence polymorphisms in the aldolase B gene. Am. J. Hum. Genet. 52, 835–840 (1993).

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