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Catalytic deficiency of human aldolase B in hereditary fructose intolerance caused by a common missense mutation

✍ Scribed by Cross, Nicholas C.P.; Tolan, Dean R.; Cox, Timothy M.


Book ID
121991367
Publisher
Elsevier Science
Year
1988
Tongue
English
Weight
912 KB
Volume
53
Category
Article
ISSN
0092-8674

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Molecular basis of hereditary fructose i
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Mutations in the human aldolase B gene that result in hereditary fructose intolerance have been characterized extensively. Although the majority of subjects have been from northern Europe, subjects from other geographical regions and ethnic groups have been identified. At present 2 1 mutations have