Literature DB >> 20668260

FUS mutations in sporadic juvenile ALS: another step toward understanding ALS pathogenesis.

David G Munoz.   

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Year:  2010        PMID： 20668260     DOI： 10.1212/WNL.0b013e3181ed9ee4

Source DB:  PubMed          Journal:  Neurology        ISSN： 0028-3878            Impact factor:   9.910


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  3 in total

1.  Aberrant localization of FUS and TDP43 is associated with misfolding of SOD1 in amyotrophic lateral sclerosis.

Authors:  Edward Pokrishevsky; Leslie I Grad; Masoud Yousefi; Jing Wang; Ian R Mackenzie; Neil R Cashman
Journal:  PLoS One       Date:  2012-04-06       Impact factor: 3.240

2.  Genotype-phenotype relationship in hereditary amyotrophic lateral sclerosis.

Authors:  Satoshi Yamashita; Yukio Ando
Journal:  Transl Neurodegener       Date:  2015-07-24       Impact factor: 8.014

Review 3.  Genotype-phenotype correlations of amyotrophic lateral sclerosis.

Authors:  Hong-Fu Li; Zhi-Ying Wu
Journal:  Transl Neurodegener       Date:  2016-02-03       Impact factor: 8.014
  3 in total

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