Author:
Denora Paola S.,Brockmann Knut,Ciccolella Marianna,Truchetto Jeremy,Stevanin Giovanni,Santorelli Filippo M.
Funder
Italian Ministry of Health
E-RARE grant from the European Union
Subject
Neurology (clinical),Neurology
Reference8 articles.
1. Clinical and genetic studies in hereditary spastic paraplegia with thin corpus callosum;Casali;Neurology,2004
2. Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum;Stevanin;Nat Genet,2007
3. The Spastic Paraplegia Rating Scale (SPRS): a reliable and valid measure of disease severity;Schüle;Neurology,2006
4. Screening of ARHSP-TCC patients expands the spectrum of SPG11 mutations and includes a large scale gene deletion;Denora;Hum Mutat,2009
5. The Mitochondrial tRNALeU(UUR) Mutation in mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes (MELAS): genetic, biochemical, and morphological correlations in skeletal muscle;Moraes;Am J Hum Genet,1992
Cited by
1 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