Found: 3
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A Japanese case of cerebellar ataxia, spastic paraparesis and deep sensory impairment associated with a novel homozygous TTC19 mutation.
- Published in:
- Journal of Human Genetics, 2015, v. 60, n. 4, p. 187, doi. 10.1038/jhg.2015.7
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- Publication type:
- Article
Diagnostic utility of whole exome sequencing in patients showing cerebellar and/or vermis atrophy in childhood.
- Published in:
- Neurogenetics, 2013, v. 14, n. 3/4, p. 225, doi. 10.1007/s10048-013-0375-8
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- Publication type:
- Article
Cerebrospinal fluid level of Nogo receptor 1 antagonist lateral olfactory tract usher substance (LOTUS) correlates inversely with the extent of neuroinflammation.
- Published in:
- 2018
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- Publication type:
- journal article