𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Molecular basis of Parkinsons’s disease linked toLRRK2mutations

✍ Scribed by Pchelina, S. N.; Emelyanov, A. K.; Usenko, T. S.


Book ID
121541503
Publisher
SP MAIK Nauka/Interperiodica
Year
2014
Tongue
English
Weight
266 KB
Volume
48
Category
Article
ISSN
0026-8933

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Molecular biology changes associated wit
✍ Yi Wei Lu; Eng-King Tan 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 104 KB

## Abstract Parkinson's disease (PD) is characterized by progressive dopaminergic neuronal loss in the substantia nigra. The recent discovery of __leucine‐rich‐repeat kinase 2__ gene (__LRRK2__) mutations in PD is significant because these mutations are the most common cause of autosomal dominant P

PLA2G6 mutations in PARK14-linked young-
✍ Chin-Song Lu; Szu-Chia Lai; Ruey-Meei Wu; Yi-Hsin Weng; Chia-Ling Huang; Rou-Sha 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 458 KB 👁 2 views

## Abstract Mutations of __PLA2G6__ gene have been lately proposed to be the causative gene for PARK14 in patients with autosomal recessive young‐onset parkinsonism (YOPD). The role of __PLA2G6__ mutations as a risk factor for Parkinson's disease is not clear. To study the __PLA2G6__ mutations in P