𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Screening for MAPT and PGRN mutations in Korean patients with PSP/CBS/FTD

✍ Scribed by Han-Joon Kim; Beom S. Jeon; Ji Young Yun; Moon-Woo Seong; Sung Sup Park; Jee-Young Lee

Book ID
116820752
Publisher
Elsevier Science
Year
2010
Tongue
English
Weight
95 KB
Volume
16
Category
Article
ISSN
1353-8020

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Novel progranulin mutation: Screening fo
Novel progranulin mutation: Screening for PGRN mutations in a Portuguese series of FTD/CBS cases
✍ Rita Joao Guerreiro; Isabel Santana; Jose Miguel Bras; Tamas Revesz; Olinda Rebe πŸ“‚ Article πŸ“… 2008 πŸ› John Wiley and Sons 🌐 English βš– 125 KB

## Abstract Mutations in the progranulin (__PGRN__) gene were recently described as the cause of ubiquitin positive frontotemporal dementia (FTD) in many families. Different frequencies of these genetic changes have been reported in diverse populations leading us to determine if these mutations wer