A new aldolase B variant, N334K, is a common cause of hereditary fructose intolerance in Yugoslavia
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics
Link
http://academic.oup.com/nar/article-pdf/18/7/1925/3833575/18-7-1925.pdf
Cited by 26 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Epidemiological aspects of hereditary fructose intolerance: A database study;Human Mutation;2021-09-24
2. Recent advances in the pathogenesis of hereditary fructose intolerance: implications for its treatment and the understanding of fructose-induced non-alcoholic fatty liver disease;Cellular and Molecular Life Sciences;2019-11-12
3. Fructosuria and recurrent hypoglycemia in a patient with a novel c.1693T>A variant in the 3′ untranslated region of the aldolase B gene;SAGE Open Medical Case Reports;2019-01
4. A Novel Frameshift Mutation of the ALDOB Gene in a Korean Girl Presenting with Recurrent Hepatitis Diagnosed as Hereditary Fructose Intolerance;Gut and Liver;2012-01-30
5. Integration of PCR-Sequencing Analysis with Multiplex Ligation-Dependent Probe Amplification for Diagnosis of Hereditary Fructose Intolerance;JIMD Reports;2012
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