A novel autosomal dominant spinocerebellar ataxia (SCA22) linked to chromosome 1p21-q23

By Chung M-y.  

Brain, Vol. 126, Iss. 6, 2003-06 ,pp. : 1293-1299

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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The role of the SCA2 trinucleotide repeat expansion in 89 autosomal dominant cerebellar ataxia families. Frequency, clinical and genetic correlates

By Giunti P   Sabbadini G   Sweeney MG   Davis MB   Veneziano L   Mantuano E   Federico A   Plasmati R   Frontali M   Wood NW  

Brain, Vol. 121, Iss. 3, 1998-03 ,pp. : 459-467

Oxford University Press

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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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A new autosomal recessive non-progressive congenital cerebellar ataxia associated with mental retardation, optic atrophy, and skin abnormalities (CAMOS) maps to chromosome 15q24-q26 in a large consanguineous Lebanese Druze family

By Delague Valérie   Bareil Corinne   Bouvagnet Patrice   Salem Nabiha   Chouery Eliane   Loiselet Jacques   Mégarbané André   Claustres Mireille  

Neurogenetics, Vol. 4, Iss. 1, 2002-03 ,pp. : 23-27

Springer Publishing Company

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