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.

DOBSON STONE, C., VELAYOS BAEZA, A., Filippone, L.a., Westbury, S., Storch, A., Erdmann, T., et al. (2004). Chorein detection for the diagnosis of chorea-acanthocytosis. ANNALS OF NEUROLOGY, 56(2), 299-302 [10.1002/ana.20200].

Chorein detection for the diagnosis of chorea-acanthocytosis

DOTTI, MARIA;FEDERICO, ANTONIO;
2004-01-01

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.
2004
DOBSON STONE, C., VELAYOS BAEZA, A., Filippone, L.a., Westbury, S., Storch, A., Erdmann, T., et al. (2004). Chorein detection for the diagnosis of chorea-acanthocytosis. ANNALS OF NEUROLOGY, 56(2), 299-302 [10.1002/ana.20200].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11365/4112
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