Absence of aprataxin gene mutations in a Greek cohort with sporadic early onset ataxia and normal GAA triplets in frataxin gene

Lack of mutations in spinocerebellar ata

Lack of mutations in spinocerebellar ataxia type 2 and 3 genes in a Taiwanese (ethnic Chinese) cohort of familial and early-onset parkinsonism

✍ Chin-Hsien Lin; Wuh-Liang Hwu; Shu-Chuan Chiang; Chun-Hwei Tai; Ruey-Meei Wu 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 95 KB 👁 2 views

## Abstract Recent reports suggest that CAG triplet expansions of spinocerebellar ataxia type 2 and 3 (__SCA2__ and __SCA3__) genes are the cause of typical levodopa‐responsive Parkinson's disease (PD) in familial cases, several of which were ethnic Chinese. To investigate the role of __SCA2__ and