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TDP-43 A315T mutation in familial motor neuron disease.

Authors :
Gitcho MA
Baloh RH
Chakraverty S
Mayo K
Norton JB
Levitch D
Hatanpaa KJ
White CL 3rd
Bigio EH
Caselli R
Baker M
Al-Lozi MT
Morris JC
Pestronk A
Rademakers R
Goate AM
Cairns NJ
Source :
Annals of neurology [Ann Neurol] 2008 Apr; Vol. 63 (4), pp. 535-8. Date of Electronic Publication: 2008 Feb 20.
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.

Details

Language :
English
ISSN :
1531-8249
Volume :
63
Issue :
4
Database :
MEDLINE
Journal :
Annals of neurology
Publication Type :
Academic Journal
Accession number :
18288693
Full Text :
https://doi.org/10.1002/ana.21344