Amyotrophic Lateral Sclerosis: An Emerging Era of Collaborative Gene Discovery-Reference-Cited by-同舟云学术

Amyotrophic Lateral Sclerosis: An Emerging Era of Collaborative Gene Discovery

Published:2007-12-05 Issue:12 Volume:2 Page:e1254
ISSN:1932-6203
Container-title:PLoS ONE
language:en
Short-container-title:PLoS ONE

Author:

Gwinn Katrina,Corriveau Roderick A.,Mitsumoto Hiroshi,Bednarz Kate,Brown Robert H.,Cudkowicz Merit,Gordon Paul H.,Hardy John,Kasarskis Edward J.,Kaufmann Petra,Miller Robert,Sorenson Eric,Tandan Rup,Traynor Bryan J.,Nash Josefina,Sherman Alex,Mailman Matthew D.,Ostell James,Bruijn Lucie,Cwik Valerie,Rich Stephen S.,Singleton Andrew,Refolo Larry,Andrews Jaime,Zhang Ran,Conwit Robin,Keller Margaret A.,

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference48 articles.

1. From Charcot to Lou Gehrig: deciphering selective motor neuron death in ALS.;DW Cleveland;Nat Rev Neurosci,2001

2. Complex genetics of amyotrophic lateral sclerosis.;CB Kunst;Am J Hum Genet,2004

3. DNA/RNA helicase gene mutations in a form of juvenile amyotrophic lateral sclerosis (ALS4).;Y-Z Chen;Am J Hum Genet,2004

4. Mutant dynactin in motor neuron disease.;I Puls;Nat Genet,2003

5. Point mutations of the p150 subunit of dynactin (DCTN1) gene in ALS.;C Munch;Neurology,2004

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