Spinocerebellar Ataxia Type 3

Description

A very rare, autosomal dominant inherited neurodegenerative disorder. Signs and symptoms include ataxia, spasticity, and abnormalities in the ocular movements.

Cell Lines

CSUXHi001-A
CSUXHi005-A
MUSIi004-A
ZZUi026-A
ZZUNEUi002-A
UKBi001-B
UKBi003-A
UKBi007-A
UKBi008-A
ZZUi004-A
ZZUi014-A