Found: 6
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A novel de novo RNF216 mutation associated with autosomal recessive Huntington‐like disorder.
- Published in:
- Annals of Clinical & Translational Neurology, 2020, v. 7, n. 5, p. 860, doi. 10.1002/acn3.51047
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- Article
Clinical features and mutation spectrum in Chinese patients with CADASIL: A multicenter retrospective study.
- Published in:
- CNS Neuroscience & Therapeutics, 2017, v. 23, n. 9, p. 707, doi. 10.1111/cns.12719
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- Article
Common genetic variants in PRRC2A are associated with both neuromyelitis optica spectrum disorder and multiple sclerosis in Han Chinese population.
- Published in:
- Journal of Neurology, 2021, v. 268, n. 2, p. 506, doi. 10.1007/s00415-020-10184-z
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- Article
No association between identified multiple sclerosis non-MHC risk loci and neuromyelitis optica.
- Published in:
- Neuroscience Bulletin, 2014, v. 30, n. 6, p. 1036, doi. 10.1007/s12264-013-1457-1
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- Article
Variants in the promoter region of CYP7A1 are associated with neuromyelitis optica but not with multiple sclerosis in the Han Chinese population.
- Published in:
- Neuroscience Bulletin, 2013, v. 29, n. 5, p. 525, doi. 10.1007/s12264-013-1347-6
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- Article
Whole-Exome Sequencing Identified a Novel Mutation in RNF216 in a Family with Gordon Holmes Syndrome.
- Published in:
- Journal of Molecular Neuroscience, 2022, v. 72, n. 4, p. 691, doi. 10.1007/s12031-021-01953-0
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- Article