A novel mouse model with impaired dynein/dynactin function develops amyotrophic lateral sclerosis (ALS)-like features in motor neurons and improves lifespan in SOD1-ALS mice

Author： Teuling Eva   van Dis Vera   Wulf Phebe S.   Haasdijk Elize D.   Akhmanova Anna   Hoogenraad Casper C.   Jaarsma Dick  

Publisher： Oxford University Press

ISSN： 1460-2083

Source： Human Molecular Genetics, Vol.17, Iss.18, 2008-09, pp. : 2849-2862

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