Human Genome Epidemiology Literature Finder
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Query Trace: Paraplegia and SLC33A1[original query] |
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A total of 220 patients with autosomal dominant spastic paraplegia do not display mutations in the SLC33A1 gene (SPG42). European journal of human genetics : EJHG 2010 Sep 18 (9): 1065-7. Schlipf Nina A, Beetz Christian, Schüle Rebecca, Stevanin Giovanni, Erichsen Anne Kjersti, Forlani Sylvie, Zaros Cécile, Karle Kathrin, Klebe Stephan, Klimpe Sven, Durr Alexandra, Otto Susanne, Tallaksen Chantal M E, Riess Olaf, Brice Alexis, Bauer Peter, Schöls Ludg |
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