| Literature DB >> 15293285 |
Carol Dobson-Stone1, Antonio Velayos-Baeza, Lea A Filippone, Sarah Westbury, Alexander Storch, Torsten Erdmann, Stephen J Wroe, Klaus L Leenders, Anthony E Lang, Maria Teresa Dotti, Antonio Federico, Saidi A Mohiddin, Lameh Fananapazir, Geoff Daniels, Adrian Danek, Anthony P Monaco.
Abstract
Chorea-acanthocytosis (ChAc) is a severe, neurodegenerative disorder that shares clinical features with Huntington's disease and McLeod syndrome. It is caused by mutations in VPS13A, which encodes a large protein called chorein. Using antichorein antisera, we found expression of chorein in all human cells analyzed. However, chorein expression was absent or noticeably reduced in ChAc patient cells, but not McLeod syndrome and Huntington's disease cells. This suggests that loss of chorein expression is a diagnostic feature of ChAc. Copyright 2004 American Neurological AssociationEntities:
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Year: 2004 PMID: 15293285 DOI: 10.1002/ana.20200
Source DB: PubMed Journal: Ann Neurol ISSN: 0364-5134 Impact factor: 10.422