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Erratum to: PARP10 deficiency manifests by severe developmental delay and DNA repair defect.
- Published in:
- 2017
- By:
- Publication type:
- Erratum
TFG associated hereditary spastic paraplegia: an addition to the phenotypic spectrum.
- Published in:
- Neurogenetics, 2017, v. 18, n. 2, p. 105, doi. 10.1007/s10048-017-0508-6
- By:
- Publication type:
- Article
Identification and functional characterization of a novel MTFMT mutation associated with selective vulnerability of the visual pathway and a mild neurological phenotype.
- Published in:
- Neurogenetics, 2017, v. 18, n. 2, p. 97, doi. 10.1007/s10048-016-0506-0
- By:
- Publication type:
- Article
Analysis of gene expression in the nervous system identifies key genes and novel candidates for health and disease.
- Published in:
- Neurogenetics, 2017, v. 18, n. 2, p. 81, doi. 10.1007/s10048-017-0509-5
- By:
- Publication type:
- Article
ADCY5-related dyskinesia presenting as familial myoclonus-dystonia.
- Published in:
- Neurogenetics, 2017, v. 18, n. 2, p. 111, doi. 10.1007/s10048-017-0510-z
- By:
- Publication type:
- Article
Recurrent KIF2A mutations are responsible for classic lissencephaly.
- Published in:
- Neurogenetics, 2017, v. 18, n. 2, p. 73, doi. 10.1007/s10048-016-0499-8
- By:
- Publication type:
- Article