NEK1 mutations and the risk of amyotrophic lateral sclerosis (ALS): a meta-analysis
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Title
NEK1 mutations and the risk of amyotrophic lateral sclerosis (ALS): a meta-analysis
Authors
Keywords
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Journal
NEUROLOGICAL SCIENCES
Volume -, Issue -, Pages -
Publisher
Springer Science and Business Media LLC
Online
2021-01-19
DOI
10.1007/s10072-020-05037-6
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Note: Only part of the references are listed.- Loss-of-function variants in NEK1 are associated with an increased risk of sporadic ALS in the Japanese population
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- Critical evaluation of the Newcastle-Ottawa scale for the assessment of the quality of nonrandomized studies in meta-analyses
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- Mutations in FUS, an RNA Processing Protein, Cause Familial Amyotrophic Lateral Sclerosis Type 6
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- The NIMA-family kinase, Nek1 affects the stability of centrosomes and ciliogenesis
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- The mammalian Nek1 kinase is involved in primary cilium formation
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- TDP-43 Mutations in Familial and Sporadic Amyotrophic Lateral Sclerosis
- (2008) J. Sreedharan et al. SCIENCE
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