𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Mutation analysis of the seven in absentia homolog 1 (SIAH1) gene in Parkinson’s disease

✍ Scribed by T. Franck; R. Krueger; D. Woitalla; T. Müller; S. Engelender; O. Riess


Publisher
Springer
Year
2006
Tongue
English
Weight
93 KB
Volume
113
Category
Article
ISSN
1435-1463

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Translated mutation in the Nurr1 gene as
✍ David A. Grimes; Fabin Han; Michel Panisset; Lemuel Racacho; Fengxia Xiao; Ruobi 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 106 KB 👁 1 views

## Abstract Multiple genes have been now identified as causing Parkinson's disease (PD). In 2003, two mutations were identified in exon 1 of the Nurr1 gene in 10 of 107 individuals with familial PD. To date, investigators have only focused on screening for these known mutations of the Nurr1 gene. A

Analysis of the glucocerebrosidase gene
✍ Christine Sato; Angharad Morgan; Anthony E. Lang; Shabnam Salehi-Rad; Toshitaka 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 184 KB 👁 1 views

## Abstract Parkinson's disease (PD) is a common progressive neurodegenerative disorder characterized clinically by a combination of motor symptoms. Identifying novel PD genetic risk factors is important for understanding its pathogenesis. A recent study suggested that up to 21% of subjects with PD