TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysis-Reference-Cited by-同舟云学术

TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysis

Published:2008-05 Issue:5 Volume:7 Page:409-416
ISSN:1474-4422
Container-title:The Lancet Neurology
language:en
Short-container-title:The Lancet Neurology

Author:

Van Deerlin Vivianna M,Leverenz James B,Bekris Lynn M,Bird Thomas D,Yuan Wuxing,Elman Lauren B,Clay Dana,Wood Elisabeth McCarty,Chen-Plotkin Alice S,Martinez-Lage Maria,Steinbart Ellen,McCluskey Leo,Grossman Murray,Neumann Manuela,Wu I-Lin,Yang Wei-Shiung,Kalb Robert,Galasko Douglas R,Montine Thomas J,Trojanowski John Q,Lee Virginia M-Y,Schellenberg Gerard D,Yu Chang-En

Publisher

Elsevier BV

Subject

Neurology (clinical)

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4. A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2;Hadano;Nat Genet,2001

5. The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis;Yang;Nat Genet,2001

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