Lack of C9ORF72 coding mutations supports a gain of function for repeat expansions in amyotrophic lateral sclerosis
Harms, Matthew B., Cady, Janet, Zaidman, Craig, Cooper, Paul, Bali, Taha, Allred, Peggy, Cruchaga, Carlos, Baughn, Michael, Libby, Ryan T., Pestronk, Alan, Goate, Alison, Ravits, John, Baloh, Robert HVolume:
34
Language:
english
Journal:
Neurobiology of Aging
DOI:
10.1016/j.neurobiolaging.2013.03.006
Date:
September, 2013
File:
PDF, 413 KB
english, 2013