Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Ataxia and PRKCG[original query] |
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Molecular genetics of hereditary spinocerebellar ataxia: mutation analysis of spinocerebellar ataxia genes and CAG/CTG repeat expansion detection in 225 Italian families. Archives of neurology 2004 May 61 (5): 727-33. Brusco Alfredo, Gellera Cinzia, Cagnoli Claudia, Saluto Alessandro, Castucci Alessia, Michielotto Chiara, Fetoni Vincenza, Mariotti Caterina, Migone Nicola, Di Donato Stefano, Taroni Fran |
New mutations in protein kinase Cgamma associated with spinocerebellar ataxia type 14. Annals of neurology 2005 Nov 58 (5): 720-9. Klebe Stephan, Durr Alexandra, Rentschler Alexander, Hahn-Barma Valerie, Abele Michael, Bouslam Naima, Schöls Ludger, Jedynak Pierre, Forlani Sylvie, Denis Elodie, Dussert Christel, Agid Yves, Bauer Peter, Globas Christoph, Wüllner Ullrich, Brice Alexis, Riess Olaf, Stevanin Giovan |
Next generation sequencing for molecular diagnosis of neurological disorders using ataxias as a model. Brain : a journal of neurology 2013 Oct 136 (Pt 10): 3106-18. Németh Andrea H, Kwasniewska Alexandra C, Lise Stefano, Parolin Schnekenberg Ricardo, Becker Esther B E, Bera Katarzyna D, Shanks Morag E, Gregory Lorna, Buck David, Zameel Cader M, Talbot Kevin, de Silva Rajith, Fletcher Nicholas, Hastings Rob, Jayawant Sandeep, Morrison Patrick J, Worth Paul, Taylor Malcolm, Tolmie John, O'Regan Mary, , Valentine Ruth, Packham Emily, Evans Julie, Seller Anneke, Ragoussis Jiann |
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