Disorders of the Pentose Phosphate Pathway and Polyol Metabolism
Author:
Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-030-67727-5_40
Reference25 articles.
1. Boyle L, Wamelink MMC, Salomons GS, et al. Mutations in TKT are the cause of a syndrome including short stature, developmental delay, and congenital heart defects. Am J Human Genetics. 2016;98:1235–42.
2. Brooks SS, Anderson S, Bhise V, et al. Further delineation of ribose-5-phosphate isomerase deficiency: report of a third case. J Child Neurol. 2018;33:784–7.
3. Carr IM, Markham AF. Molecular genetic analysis of the human sorbitol dehydrogenase gene. Mamm Genome. 1995;6:645–52.
4. Engelke UFH, Zijlstra FSM, Mochel F, et al. Mitochondrial involvement and erythronic acid as a novel biomarker in transaldolase deficiency. Biochim Biophys Acta. 2010;1802:1028–35.
5. Hammes HP. Pathophysiological mechanisms of diabetic angiopathy. J Diabetes Complicat. 2003;17:16–9.
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