Human Genome Epidemiology Literature Finder
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Records 1 - 5 (of 5 Records) |
| Query Trace: Paraplegia and ZFYVE26[original query] |
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| Overlapping phenotypes in complex spastic paraplegias SPG11, SPG15, SPG35 and SPG48. Brain : a journal of neurology 2014 Jul 137 (Pt 7): 1907-20. Pensato Viviana, Castellotti Barbara, Gellera Cinzia, Pareyson Davide, Ciano Claudia, Nanetti Lorenzo, Salsano Ettore, Piscosquito Giuseppe, Sarto Elisa, Eoli Marica, Moroni Isabella, Soliveri Paola, Lamperti Elena, Chiapparini Luisa, Di Bella Daniela, Taroni Franco, Mariotti Cateri |
| ALS5/SPG11/KIAA1840 mutations cause autosomal recessive axonal Charcot-Marie-Tooth disease. Brain : a journal of neurology 2015 Nov . Montecchiani Celeste, Pedace Lucia, Lo Giudice Temistocle, Casella Antonella, Mearini Marzia, Gaudiello Fabrizio, Pedroso José L, Terracciano Chiara, Caltagirone Carlo, Massa Roberto, St George-Hyslop Peter H, Barsottini Orlando G P, Kawarai Toshitaka, Orlacchio Anton |
| Molecular analysis and clinical diversity of distal hereditary motor neuropathy. European journal of neurology 2020 4 27 (7): 1319-1326. Liu X, Duan X, Zhang Y, Sun A, Fan |
| Investigating ZFYVE26 mutations in a Taiwanese cohort with hereditary spastic paraplegia. Journal of the Formosan Medical Association = Taiwan yi zhi 2021 2 121 (1 Pt 1): 126-133. Hsu Shao-Lun, Lu Yi-Jiun, Tsai Yu-Shuen, Chao Hua-Chuan, Fuh Jong-Ling, Liao Yi-Chu, Lee Yi-Chu |
| [Genetic distribution in Chinese patients with hereditary peripheral neuropathy]. Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences 2022 10 54 (5): 874-883. Liu X X, Duan X H, Zhang S, Sun A P, Zhang Y S, Fan D |
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