Exome sequencing to identify de novo mutations in sporadic ALS trios-Reference-Cited by-同舟云学术

Exome sequencing to identify de novo mutations in sporadic ALS trios

Published:2013-05-26 Issue:7 Volume:16 Page:851-855
ISSN:1097-6256
Container-title:Nature Neuroscience
language:en
Short-container-title:Nat Neurosci

Author:

Chesi Alessandra,Staahl Brett T,Jovičić Ana,Couthouis Julien,Fasolino Maria,Raphael Alya R,Yamazaki Tomohiro,Elias Laura,Polak Meraida,Kelly Crystal,Williams Kelly L,Fifita Jennifer A,Maragakis Nicholas J,Nicholson Garth A,King Oliver D,Reed Robin,Crabtree Gerald R,Blair Ian P,Glass Jonathan D,Gitler Aaron D

Publisher

Springer Science and Business Media LLC

Subject

General Neuroscience

Link

http://www.nature.com/articles/nn.3412.pdf

Reference56 articles.

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2. Sreedharan, J. et al. TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis. Science 319, 1668–1672 (2008).

3. Vance, C. et al. Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6. Science 323, 1208–1211 (2009).

4. Kwiatkowski, T.J. et al. Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis. Science 323, 1205–1208 (2009).

5. Johnson, J.O. et al. Exome sequencing reveals VCP mutations as a cause of familial ALS. Neuron 68, 857–864 (2010).

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