CAG repeat expansion in the TATA box-binding protein gene causes autosomal dominant cerebellar ataxia

By Brice A.  

Brain, Vol. 124, Iss. 10, 2001-10 ,pp. : 1939-1947

Oxford University Press

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Mapping of the SCA23 locus involved in autosomal dominant cerebellar ataxia to chromosome region 20p13-12.3

By Verbeek D. S.  

Brain, Vol. 127, Iss. 11, 2004-11 ,pp. : 2551-2557

Oxford University Press

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SCA28, a novel form of autosomal dominant cerebellar ataxia on chromosome 18p11.22–q11.2

By Cagnoli Claudia   Mariotti Caterina   Seri Marco   Brussino Alessandro   Michielotto Chiara   Grisoli Marina   Di Bella Daniela   Migone Nicola   Gellera Cinzia  

Brain, Vol. 129, Iss. 1, 2006-01 ,pp. : 235-242

Oxford University Press

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Autosomal dominant cerebellar ataxia type I MRI-based volumetry of posterior fossa structures and basal ganglia in spinocerebellar ataxia types 1, 2 and 3

By Klockgether T   Skalej M   Wedekind D   Luft AR   Welte D   Schulz JB   Abele M   Bürk K   Laccone F   Brice A   Dichgans J  

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Basal ganglia involvement of a patient with SCA 17: A new form of autosomal dominant spinocerebellar ataxia

By Günther P.   Storch A.   Schwarz J.   Sabri O.   Steinbach P.   Wagner A.   Hesse S.  

Journal of Neurology, Vol. 251, Iss. 7, 2004-07 ,pp. : 896-897

Springer Publishing Company

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