Author:
Nishino Ichizo,Spinazzola Antonella,Hirano Michio
Subject
Genetics(clinical),Clinical Neurology,Neurology,Pediatrics, Perinatology, and Child Health
Reference11 articles.
1. Myo-, neuro-, gastrointestinal encephalopathy (MNGIE syndrome) due to partial deficiency of cytochrome-c-oxidase. A new mitochondrial multisystem disorder;Bardosi;Acta Neuropathol (Berl),1987
2. Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): clinical, biochemical, and genetic features of an autosomal recessive mitochondrial disorder;Hirano;Neurology,1994
3. Mitochondrial neurogastrointestinal encephalomyopathy syndrome maps to chromosome 22q13.32–qter;Hirano;Am J Hum Genet,1998
4. Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder;Nishino;Science,1999
5. MNGIE: an autosomal recessive disorder due to thymidine phosphorylase mutations;Nishino;Ann Neurol,2000
Cited by
65 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