𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Contribution of glucocerebrosidase mutation in a large cohort of sporadic Parkinson’s disease in Taiwan

✍ Scribed by C.-L. Huang; Y.-H. Wu-Chou; S.-C. Lai; H.-C. Chang; T.-H. Yeh; Y.-H. Weng; R.-S. Chen; Y.-Z. Huang; C.-S. Lu

Book ID
111066673
Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
105 KB
Volume
18
Category
Article
ISSN
1351-5101

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Lack of G2019S LRRK2 mutation in a cohor
Lack of G2019S LRRK2 mutation in a cohort of Taiwanese with sporadic Parkinson's disease
✍ Hon-Chung Fung; Chiung-Mei Chen; John Hardy; Dena Hernandez; Andrew Singleton; Y 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 46 KB

## Abstract Mutations in the leucine‐rich repeat kinase 2 (__LRRK2__) gene have been shown to cause autosomal dominant and sporadic Parkinson's disease (PD). We report here the frequency of a common heterozygous mutation, 2877510G>A, which produces a glycine‐to‐serine amino acid substitution at cod