Spinocerebellar ataxia type 17 is caused by mutations in the TATA-box binding protein

By Zühlke Christine  

The Cerebellum, Vol. 6, Iss. 4, 2007-01 ,pp. : 300-307

Informa Healthcare

Access to resources Recommend Favorite

A new autosomal recessive spastic ataxia associated with frequent white matter changes maps to 2q33–34

By Thiffault I.   Rioux M. F.   Tetreault M.   Jarry J.   Loiselle L.   Poirier J.   Gros-Louis F.   Mathieu J.   Vanasse M.   Rouleau G. A.   Bouchard J. P.   Lesage J.   Brais B.  

Brain, Vol. 129, Iss. 9, 2006-09 ,pp. : 2332-2340

Oxford University Press

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite

Retinal Imaging in Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay

By Nethisinghe Suran   Clayton Lisa   Vermeer Sascha   Chapple J. Paul   Reilly Mary   Bremner Fion   Giunti Paola  

Neuro-Ophthalmology, Vol. 35, Iss. 4, 2011-08 ,pp. : 197-201

Informa Healthcare

Access to resources Recommend Favorite