TDP-43A315T mutation in familial motor neuron disease-Reference-Cited by-同舟云学术

TDP-43A315T mutation in familial motor neuron disease

Published:2008-04 Issue:4 Volume:63 Page:535-538
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Gitcho Michael A.,Baloh Robert H.,Chakraverty Sumi,Mayo Kevin,Norton Joanne B.,Levitch Denise,Hatanpaa Kimmo J.,White Charles L.,Bigio Eileen H.,Caselli Richard,Baker Matt,Al-Lozi Muhammad T.,Morris John C.,Pestronk Alan,Rademakers Rosa,Goate Alison M.,Cairns Nigel J.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference14 articles.

1. TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis;Arai;Biochem Biophys Res Commun,2006

2. Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis;Neumann;Science,2006

3. TDP-43 in familial and sporadic frontotemporal lobar degeneration with ubiquitin inclusions;Cairns;Am J Pathol,2007

4. Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations;Mackenzie;Ann Neurol,2007

5. Genetic aspects of amyotrophic lateral sclerosis;Siddique;Adv Neurol,2002

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