Open AccessGain and loss of function of ALS-related mutations of TARDBP (TDP-43) cause motor deficits in vivo
Author(s) -
E. Kabashi,
L. Lin,
M. L. Tradewell,
P. A. Dion,
V. Bercier,
P. Bourgouin,
D. Rochefort,
S. B. Hadj,
H. D. Durham,
C. V. Velde,
G. A. Rouleau,
Pierre Drapeau
Publication year - 2010
Publication title -
human molecular genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.811
H-Index - 276
eISSN - 1460-2083
pISSN - 0964-6906
DOI - 10.1093/hmg/ddq203
Subject(s) - biology , tardbp , loss function , in vivo , genetics , amyotrophic lateral sclerosis , mutation , gain of function , motor function , function (biology) , gene , phenotype , medicine , disease , sod1 , physical medicine and rehabilitation , mutant
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom