Mitochondrial neurogastrointestinal encephalomyopathy: An autosomal recessive disorder due to thymidine phosphorylase mutations
Year: 2000
Type: article
Study design: Observational Study
Source: Annals of Neurology
Authors: Ichizo Nishino, Antonella Spinazzola, Alexandros Papadimitriou, Simon Hammans, Israel Steiner, Cecil D. Hahn, Anne M. Connolly, Alain Verloes, Jo�o Guimar�es, 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
Institutions: Columbia University Irving Medical Center, Columbia University, University of Thessaly, Hadassah Medical Center, University of Toronto, Hospital for Sick Children, Washington University in St. Louis, University of Liège, Hospital de Egas Moniz, Centre Hospitalier Universitaire Vaudois, University of Lausanne, Tokai University, University of Florence, Lahey Hospital and Medical Center, University of Medicine and Dentistry of New Jersey, National Center of Neurology and Psychiatry, National Institute of Neuroscience, Northwestern University, Northwestern Medicine
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W2139144665