𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Simultaneous analysis of selected mutations in SNCA and PARK2 genes in patients with Parkinsons disease

✍ Scribed by Półrolniczak, Anna; Dorszewska, Jolanta; Białek, Paweł; Florczak-Wyspiańska, Jolanta; Owecki, Michał; Kozubski, Wojciech

Book ID
122141601
Publisher
Elsevier
Year
2011
Tongue
English
Weight
50 KB
Volume
63
Category
Article
ISSN
1734-1140

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Genetic etiology of Parkinson disease as
Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation update
✍ Karen Nuytemans; Jessie Theuns; Marc Cruts; Christine Van Broeckhoven 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 290 KB 👁 2 views

To date, molecular genetic analyses have identified over 500 distinct DNA variants in five disease genes associated with familial Parkinson disease; α-__synuclein__ (__SNCA__), __parkin__ (__PARK2__), __PTEN-induced putative kinase 1__ (__PINK1__), __DJ-1__ (__PARK7__), and __Leucine-rich repeat kin