Spinocerebellar ataxia type 7 (SCA7): first report of a systematic neuropathological study of the brain of a patient with a very short expanded CAG-repeat.

Rüb, U; Brunt, E R; Gierga, K; Seidel, K; Schultz, C; Schöls, L; Auburger, G; Heinsen, H; Ippel, P F; Glimmerveen, W F; Wittebol-Post, D; Arai, K; Deller, T; de Vos, R A I

Rüb, U; Brunt, E R; Gierga, K; Seidel, K; Schultz, C; Schöls, L; Auburger, G; Heinsen, H; Ippel, P F; Glimmerveen, W F; Wittebol-Post, D; Arai, K; Deller, T; de Vos, R A I.

Affiliation

Rüb U; Institute for Clinical Neuroanatomy, J.W. Goethe University, Frankfurt/Main, Germany. U.Rueb@em.uni-frankfurt.de

Brain Pathol ; 15(4): 287-95, 2005 Oct.

Article in En | MEDLINE | ID: mdl-16389941

Subject(s)

Brain/pathology; Spinocerebellar Ataxias/pathology; Aged; Female; Humans; Immunohistochemistry; Nerve Degeneration/pathology; Retina/pathology; Spinocerebellar Ataxias/genetics; Trinucleotide Repeat Expansion

Fulltext

XML

PubMed Links

Search on Google

Full text: 1 Database: MEDLINE Main subject: Brain / Spinocerebellar Ataxias Limits: Aged / Female / Humans Language: En Year: 2005 Type: Article

Fulltext

XML

PubMed Links

Search on Google

Full text: 1 Database: MEDLINE Main subject: Brain / Spinocerebellar Ataxias Limits: Aged / Female / Humans Language: En Year: 2005 Type: Article