Author:
Balfoort Berith M.,Buijs Mark J.N.,ten Asbroek Anneloor L.M.A.,Bergen Arthur A.B.,Boon Camiel J.F.,Ferreira Elise A.,Houtkooper Riekelt H.,Wagenmakers Margreet A.E.M.,Wanders Ronald J.A.,Waterham Hans R.,Timmer Corrie,van Karnebeek Clara D.,Brands Marion M.
Subject
Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism
Reference77 articles.
1. Deficit of human ornithine aminotransferase in gyrate atrophy: molecular, cellular, and clinical aspects;Montioli;Biochim. Biophys. Acta, Proteins Proteomics,1869
2. Ornithine aminotransferase, an important Glutamate-Metabolizing enzyme at the crossroads of multiple metabolic pathways;Ginguay;Biology (Basel),2017
3. Vitamin B6-responsive ornithine aminotransferase deficiency with a novel mutation G237D;Ohkubo;Tohoku J. Exp. Med.,2005
4. Ophthalmologic heterogeneity in subjects with gyrate atrophy of choroid and retina harboring the L402P mutation of ornithine aminotransferase;Peltola;Ophthalmology.,2001
5. Correction of ornithine accumulation prevents retinal degeneration in a mouse model of gyrate atrophy of the choroid and retina;Wang;Proc. Natl. Acad. Sci. U. S. A.,2000
Cited by
13 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