The occurrence of mutations inFUSin a Belgian cohort of patients with familial ALS
Author:
Publisher
Wiley
Subject
Clinical Neurology,Neurology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1468-1331.2009.02859.x/fullpdf
Reference8 articles.
1. Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis;Kwiatkowski;Science,2009
2. Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6;Vance;Science,2009
3. Two Italian kindreds with familial amyotrophic lateral sclerosis due to FUS mutation;Chio;Neurobiol Aging,2009
4. D90A heterozygosity in the SOD1 gene is associated with familial and apparently sporadic amyotrophic lateral sclerosis;Robberecht;Neurology,1996
5. Mutational analysis of the Cu/Zn superoxide dismutase gene in 23 familial and 69 sporadic cases of amyotrophic lateral sclerosis in Belgium;Aguirre;Eur J Hum Genet,1999
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