Mitochondrial neurogastrointestinal encephalomyopathy: An autosomal recessive disorder due to thymidine phosphorylase mutations

✍ Scribed by Ichizo Nishino; Antonella Spinazzola; Alexandros Papadimitriou; Simon Hammans; Israel Steiner; Cecil D. Hahn; Anne M. Connolly; Alain Verloes; João Guimarães; Ivan Maillard; Hitoshi Hamano; M. Alice Donati; Carol E. Semrad; James A. Russell; Antonio L. Andreu; Giorgos M. Hadjigeorgiou; Tuan H. Vu; Saba Tadesse; Torbjoern G. Nygaard; Ikuya Nonaka; Ikuo Hirano; Eduardo Bonilla; Lewis P. Rowland; Salvatore DiMauro; Michio Hirano

• Book ID: 102681831
• Publisher: John Wiley and Sons
• Year: 2000
• Tongue: English
• Weight: 748 KB
• Volume: 47
• Category: Article
• ISSN: 0364-5134
• DOI: 10.1002/1531-8249(200006)47:6<792::aid-ana12>3.0.co;2-y