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7. Spinocerebellar ataxia with sensory neuropathy (SCA25). Stevanin G; Broussolle E; Streichenberger N; Kopp N; Brice A; Durr A Cerebellum; 2005; 4(1):58-61. PubMed ID: 15895562 [TBL] [Abstract][Full Text] [Related]
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10. SCA15 due to large ITPR1 deletions in a cohort of 333 white families with dominant ataxia. Marelli C; van de Leemput J; Johnson JO; Tison F; Thauvin-Robinet C; Picard F; Tranchant C; Hernandez DG; Huttin B; Boulliat J; Sangla I; Marescaux C; Brique S; Dollfus H; Arepalli S; Benatru I; Ollagnon E; Forlani S; Hardy J; Stevanin G; Dürr A; Singleton A; Brice A Arch Neurol; 2011 May; 68(5):637-43. PubMed ID: 21555639 [TBL] [Abstract][Full Text] [Related]
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13. Pontine atrophy in spinocerebellar ataxia type 6. Sugawara M; Toyoshima I; Wada C; Kato K; Ishikawa K; Hirota K; Ishiguro H; Kagaya H; Hirata Y; Imota T; Ogasawara M; Masamune O Eur Neurol; 2000; 43(1):17-22. PubMed ID: 10601803 [TBL] [Abstract][Full Text] [Related]
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18. Molecular genetics of spinocerebellar ataxia type 8 (SCA8). Mosemiller AK; Dalton JC; Day JW; Ranum LP Cytogenet Genome Res; 2003; 100(1-4):175-83. PubMed ID: 14526178 [TBL] [Abstract][Full Text] [Related]