Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Ataxia and REEP1[original query] |
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REEP1 mutations in SPG31: frequency, mutational spectrum, and potential association with mitochondrial morpho-functional dysfunction. Human mutation 2011 Oct 32 (10): 1118-27. Goizet Cyril, Depienne Christel, Benard Giovanni, Boukhris Amir, Mundwiller Emeline, Solé Guilhem, Coupry Isabelle, Pilliod Julie, Martin-Négrier Marie-Laure, Fedirko Estelle, Forlani Sylvie, Cazeneuve Cécile, Hannequin Didier, Charles Perrine, Feki Imed, Pinel Jean-François, Ouvrard-Hernandez Anne-Marie, Lyonnet Stanislas, Ollagnon-Roman Elisabeth, Yaouanq Jacqueline, Toutain Annick, Dussert Christelle, Fontaine Bertrand, Leguern Eric, Lacombe Didier, Durr Alexandra, Rossignol Rodrigue, Brice Alexis, Stevanin Giovan |
Clinical Features and Genetic Spectrum of Patients With Clinically Suspected Hereditary Progressive Spastic Paraplegia. Frontiers in neurology 2022 5 13 872927. Shi Yuzhi, Wang An, Chen Bin, Wang Xingao, Niu Songtao, Li Wei, Li Shaowu, Zhang Zaiqia |
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