Found: 4
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Expanding the β-III Spectrin-Associated Phenotypes toward Non-Progressive Congenital Ataxias with Neurodegeneration.
- Published in:
- International Journal of Molecular Sciences, 2021, v. 22, n. 5, p. 2505, doi. 10.3390/ijms22052505
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- Publication type:
- Article
De novo mutations in KIF1A cause progressive encephalopathy and brain atrophy.
- Published in:
- Annals of Clinical & Translational Neurology, 2015, v. 2, n. 6, p. 623, doi. 10.1002/acn3.198
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- Publication type:
- Article
Hypomyelination with atrophy of the basal ganglia and cerebellum: further delineation of the phenotype and genotype-phenotype correlation.
- Published in:
- 2014
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- Publication type:
- journal article
Hypomyelination with atrophy of the basal ganglia and cerebellum: further delineation of the phenotype and genotype–phenotype correlation.
- Published in:
- Brain: A Journal of Neurology, 2014, v. 137, n. 7, p. 1921
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- Publication type:
- Article