Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis-Reference-Cited by-同舟云学术

Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis

Published:2012-07-15 Issue:7412 Volume:488 Page:499-503
ISSN:0028-0836
Container-title:Nature
language:en
Short-container-title:Nature

Author:

Wu Chi-Hong,Fallini Claudia,Ticozzi Nicola,Keagle Pamela J.,Sapp Peter C.,Piotrowska Katarzyna,Lowe Patrick,Koppers Max,McKenna-Yasek Diane,Baron Desiree M.,Kost Jason E.,Gonzalez-Perez Paloma,Fox Andrew D.,Adams Jenni,Taroni Franco,Tiloca Cinzia,Leclerc Ashley Lyn,Chafe Shawn C.,Mangroo Dev,Moore Melissa J.,Zitzewitz Jill A.,Xu Zuo-Shang,van den Berg Leonard H.,Glass Jonathan D.,Siciliano Gabriele,Cirulli Elizabeth T.,Goldstein David B.,Salachas Francois,Meininger Vincent,Rossoll Wilfried,Ratti Antonia,Gellera Cinzia,Bosco Daryl A.,Bassell Gary J.,Silani Vincenzo,Drory Vivian E.,Brown Jr Robert H.,Landers John E.

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/nature11280.pdf

Reference39 articles.

1. Kabashi, E. et al. TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis. Nature Genet. 40, 572–574 (2008)

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

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

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