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Whole-exome sequencing confirms implication of VPS13D as a potential cause of progressive spastic ataxia.
- Published in:
- 2022
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- Publication type:
- journal article
Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders.
- Published in:
- Nature Genetics, 2007, v. 39, n. 1, p. 25, doi. 10.1038/ng1933
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- Publication type:
- Article
The Planar Polarity Protein Scribble1 Is Essential for Neuronal Plasticity and Brain Function.
- Published in:
- Journal of Neuroscience, 2010, v. 30, n. 29, p. 9738, doi. 10.1523/JNEUROSCI.6007-09.2010
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- Publication type:
- Article
New practical definitions for the diagnosis of autosomal recessive spastic ataxia of Charlevoix-Saguenay.
- Published in:
- 2015
- By:
- Publication type:
- journal article
Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: A Gradient of Severity in Cognitive Impairments.
- Published in:
- PLoS Genetics, 2014, v. 10, n. 9, p. 1, doi. 10.1371/journal.pgen.1004580
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- Publication type:
- Article
CYP2U1 activity is altered by missense mutations in hereditary spastic paraplegia 56.
- Published in:
- Human Mutation, 2018, v. 39, n. 1, p. 140, doi. 10.1002/humu.23359
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- Publication type:
- Article
An investigation of ribosomal protein L10 gene in autism spectrum disorders.
- Published in:
- BMC Medical Genetics, 2009, v. 10, p. 1, doi. 10.1186/1471-2350-10-7
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- Publication type:
- Article