학술논문
Progranulin null mutations in both sporadic and familial frontotemporal dementia
Document Type
Article
Author
Le Ber, I.; Camuzat, A.; Duyckaerts, C.; Verpillat, P.; Brice, A.; Dubois, B.; Lacomblez, L.; Salachas, F.; Van Der Zee, J.; Gijselinck, U.; De Pooter, T.; Van Den Broeck, M.; Cruts, M.; Van Broeckhoven, C.; Hannequin, D.; Campion, D.; Puel, M.; Laquerrière, A.; Sellal, F.; Vercelletto, M.; Thomas-Antérion, C.; Michel, B.-F.; Golfier, V.; Didic, M.; Clerget-Darpoux, F.; Defer, G.; Desnuelle, C.; Pasquier, F.; Camu, W.
Source
In: Human Mutation . (Human Mutation, September 2007, 28(9):846-855)
Subject
Language
English
ISSN
10597794