Mutations in FUS are the most frequent genetic cause in juvenile sporadic ALS patients of Chinese origin
Published 2016 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Mutations in FUS are the most frequent genetic cause in juvenile sporadic ALS patients of Chinese origin
Authors
Keywords
-
Journal
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
Volume 17, Issue 3-4, Pages 249-252
Publisher
Informa UK Limited
Online
2016-03-14
DOI
10.3109/21678421.2016.1143012
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- De novo FUS mutations are the most frequent genetic cause in early-onset German ALS patients
- (2015) Annemarie Hübers et al. NEUROBIOLOGY OF AGING
- A novel P66S mutation in exon 3 of the SOD1 gene with early onset and rapid progression
- (2012) Dušan Keckarević et al. Amyotrophic Lateral Sclerosis
- SOD1, ANG, TARDBP and FUS mutations in amyotrophic lateral sclerosis: A United States clinical testing lab experience
- (2012) Jeffrey A. Brown et al. Amyotrophic Lateral Sclerosis
- ALSoD: A user-friendly online bioinformatics tool for amyotrophic lateral sclerosis genetics
- (2012) Olubunmi Abel et al. HUMAN MUTATION
- De novo FUS gene mutations are associated with juvenile-onset sporadic amyotrophic lateral sclerosis in China
- (2012) Zhang-Yu Zou et al. NEUROBIOLOGY OF AGING
- Contribution of major amyotrophic lateral sclerosis genes to the etiology of sporadic disease
- (2012) S. Lattante et al. NEUROLOGY
- Identification of novelFUSmutations in sporadic cases of amyotrophic lateral sclerosis
- (2011) Veronique V. Belzil et al. Amyotrophic Lateral Sclerosis
- Sporadic juvenile amyotrophic lateral sclerosis caused by mutant FUS/TLS: possible association of mental retardation with this mutation
- (2011) Satoshi Yamashita et al. JOURNAL OF NEUROLOGY
- Amyotrophic lateral sclerosis
- (2011) Matthew C Kiernan et al. LANCET
- P525L FUS mutation is consistently associated with a severe form of juvenile Amyotrophic Lateral Sclerosis
- (2011) Amelia Conte et al. NEUROMUSCULAR DISORDERS
- Senataxin mutations and amyotrophic lateral sclerosis
- (2010) Michio Hirano et al. Amyotrophic Lateral Sclerosis
- Nuclear transport impairment of amyotrophic lateral sclerosis-linked mutations in FUS/TLS
- (2010) Daisuke Ito et al. ANNALS OF NEUROLOGY
- Extensive FUS-Immunoreactive Pathology in Juvenile Amyotrophic Lateral Sclerosis with Basophilic Inclusions
- (2010) Eric J. Huang et al. BRAIN PATHOLOGY
- ALS-associated fused in sarcoma (FUS) mutations disrupt Transportin-mediated nuclear import
- (2010) Dorothee Dormann et al. EMBO JOURNAL
- De novo truncating FUS gene mutation as a cause of sporadic amyotrophic lateral sclerosis
- (2010) Mariely DeJesus-Hernandez et al. HUMAN MUTATION
- Juvenile ALS with basophilic inclusions is a FUS proteinopathy with FUS mutations
- (2010) D. Baumer et al. NEUROLOGY
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreFind the ideal target journal for your manuscript
Explore over 38,000 international journals covering a vast array of academic fields.
Search