DPP6 gene disruption in a family with Gilles de la Tourette syndrome.
- Published in:
- Neurogenetics, 2014, v. 15, n. 4, p. 237, doi. 10.1007/s10048-014-0418-9
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- Publication type:
- Article
Works matching IS 13646745 AND DT 2014 AND VI 15 AND IP 4
Results: 8
1
2
Analysis of dynein intermediate chains, light intermediate chains and light chains in a cohort of hereditary peripheral neuropathies.
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- Neurogenetics, 2014, v. 15, n. 4, p. 229, doi. 10.1007/s10048-014-0414-0
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- Publication type:
- Article
3
DNA repair abnormalities leading to ataxia: shared neurological phenotypes and risk factors.
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- Neurogenetics, 2014, v. 15, n. 4, p. 217, doi. 10.1007/s10048-014-0415-z
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- Publication type:
- Article
4
Genes and Gene Networks Implicated in Aggression Related Behaviour.
- Published in:
- Neurogenetics, 2014, v. 15, n. 4, p. 255, doi. 10.1007/s10048-014-0417-x
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- Publication type:
- Article
5
miR-338-3p is over-expressed in blood, CFS, serum and spinal cord from sporadic amyotrophic lateral sclerosis patients.
- Published in:
- Neurogenetics, 2014, v. 15, n. 4, p. 243, doi. 10.1007/s10048-014-0420-2
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- Publication type:
- Article
6
A quantitative transcriptome reference map of the normal human brain.
- Published in:
- Neurogenetics, 2014, v. 15, n. 4, p. 267, doi. 10.1007/s10048-014-0419-8
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- Publication type:
- Article
7
Acknowledgement to Referees 2013/2014.
- Published in:
- Neurogenetics, 2014, v. 15, n. 4, p. 295, doi. 10.1007/s10048-014-0423-z
- Publication type:
- Article
8
A novel mutation in the CSF1R gene causes a variable leukoencephalopathy with spheroids.
- Published in:
- Neurogenetics, 2014, v. 15, n. 4, p. 289, doi. 10.1007/s10048-014-0413-1
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- Publication type:
- Article