Degeneration of ingestion-related brainstem nuclei in spinocerebellar ataxia type 2, 3, 6 and 7-Reference-Cited by-同舟云学术

Degeneration of ingestion-related brainstem nuclei in spinocerebellar ataxia type 2, 3, 6 and 7

Published:2006-12 Issue:6 Volume:32 Page:635-649
ISSN:0305-1846
Container-title:Neuropathology and Applied Neurobiology
language:en
Short-container-title:Neuropathol Appl Neurobiol

Author:

Rüb U.,Brunt E. R.,Petrasch-Parwez E.,Schöls L.,Theegarten D.,Auburger G.,Seidel K.,Schultz C.,Gierga K.,Paulson H.,van Broeckhoven C.,Deller T.,de Vos R. A. I.

Publisher

Wiley

Subject

Physiology (medical),Clinical Neurology,Neurology,Histology,Pathology and Forensic Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2990.2006.00772.x/fullpdf

Reference57 articles.

1. Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion

2. Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies)

3. Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats

4. Cytoplasmic and nuclear polyglutamine aggregates in SCA6 Purkinje cells

5. CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1

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