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10. A new dominant spinocerebellar ataxia linked to chromosome 19q13.4-qter. Brkanac Z; Bylenok L; Fernandez M; Matsushita M; Lipe H; Wolff J; Nochlin D; Raskind WH; Bird TD Arch Neurol; 2002 Aug; 59(8):1291-5. PubMed ID: 12164726 [TBL] [Abstract][Full Text] [Related]
11. An autosomal dominant ataxia maps to 19q13: Allelic heterogeneity of SCA13 or novel locus? Waters MF; Fee D; Figueroa KP; Nolte D; Müller U; Advincula J; Coon H; Evidente VG; Pulst SM Neurology; 2005 Oct; 65(7):1111-3. PubMed ID: 16135769 [TBL] [Abstract][Full Text] [Related]
12. Mapping of the SCA23 locus involved in autosomal dominant cerebellar ataxia to chromosome region 20p13-12.3. Verbeek DS; van de Warrenburg BP; Wesseling P; Pearson PL; Kremer HP; Sinke RJ Brain; 2004 Nov; 127(Pt 11):2551-7. PubMed ID: 15306549 [TBL] [Abstract][Full Text] [Related]
13. Spinocerebellar ataxia with sensory neuropathy (SCA25) maps to chromosome 2p. Stevanin G; Bouslam N; Thobois S; Azzedine H; Ravaux L; Boland A; Schalling M; Broussolle E; Dürr A; Brice A Ann Neurol; 2004 Jan; 55(1):97-104. PubMed ID: 14705117 [TBL] [Abstract][Full Text] [Related]
14. Two Italian families with ITPR1 gene deletion presenting a broader phenotype of SCA15. Di Gregorio E; Orsi L; Godani M; Vaula G; Jensen S; Salmon E; Ferrari G; Squadrone S; Abete MC; Cagnoli C; Brussino A; Brusco A Cerebellum; 2010 Mar; 9(1):115-23. PubMed ID: 20082166 [TBL] [Abstract][Full Text] [Related]
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16. Spinocerebellar ataxia type 15 (sca15) maps to 3p24.2-3pter: exclusion of the ITPR1 gene, the human orthologue of an ataxic mouse mutant. Knight MA; Kennerson ML; Anney RJ; Matsuura T; Nicholson GA; Salimi-Tari P; Gardner RJ; Storey E; Forrest SM Neurobiol Dis; 2003 Jul; 13(2):147-57. PubMed ID: 12828938 [TBL] [Abstract][Full Text] [Related]
17. Refinement of the spinocerebellar ataxia type 4 locus in a large German family and exclusion of CAG repeat expansions in this region. Hellenbroich Y; Bubel S; Pawlack H; Opitz S; Vieregge P; Schwinger E; Zühlke C J Neurol; 2003 Jun; 250(6):668-71. PubMed ID: 12796826 [TBL] [Abstract][Full Text] [Related]
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20. Clinical and genetic characterizations of 16q-linked autosomal dominant spinocerebellar ataxia (AD-SCA) and frequency analysis of AD-SCA in the Japanese population. Nozaki H; Ikeuchi T; Kawakami A; Kimura A; Koide R; Tsuchiya M; Nakmura Y; Mutoh T; Yamamoto H; Nakao N; Sahashi K; Nishizawa M; Onodera O Mov Disord; 2007 Apr; 22(6):857-62. PubMed ID: 17357132 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]