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TDP-43 A315T mutation in familial motor neuron disease.

Authors :
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.
Source :
Annals of Neurology; Apr2008, Vol. 63 Issue 4, p535-538, 4p
Publication Year :
2008

Abstract

To identify novel causes of familial neurodegenerative diseases, we extended our previous studies of TAR DNA-binding protein 43 (TDP-43) proteinopathies to investigate TDP-43 as a candidate gene in familial cases of motor neuron disease. Sequencing of the TDP-43 gene led to the identification of a novel missense mutation, Ala-315-Thr, which segregates with all affected members of an autosomal dominant motor neuron disease family. The mutation was not found in 1,505 healthy control subjects. The discovery of a missense mutation in TDP-43 in a family with dominantly inherited motor neuron disease provides evidence of a direct link between altered TDP-43 function and neurodegeneration. Ann Neurol 2008 [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
03645134
Volume :
63
Issue :
4
Database :
Complementary Index
Journal :
Annals of Neurology
Publication Type :
Academic Journal
Accession number :
71235310
Full Text :
https://doi.org/10.1002/ana.21344