Acknowledgement to referees 2018/2019.
- Published in:
- 2019
- Publication type:
- Calendar
Works matching IS 13646745 AND DT 2019 AND VI 20 AND IP 4
Results: 7
1
2
Frequency of the LRRK2 G2019S mutation in South African patients with Parkinson's disease.
- Published in:
- Neurogenetics, 2019, v. 20, n. 4, p. 215, doi. 10.1007/s10048-019-00588-z
- By:
- Publication type:
- Article
3
VPS53 gene is associated with a new phenotype of complicated hereditary spastic paraparesis.
- Published in:
- Neurogenetics, 2019, v. 20, n. 4, p. 187, doi. 10.1007/s10048-019-00586-1
- By:
- Publication type:
- Article
4
Nervous NDRGs: the N-myc downstream–regulated gene family in the central and peripheral nervous system.
- Published in:
- Neurogenetics, 2019, v. 20, n. 4, p. 173, doi. 10.1007/s10048-019-00587-0
- By:
- Publication type:
- Article
5
Identification and characterization of novel and rare susceptible variants in Indian amyotrophic lateral sclerosis patients.
- Published in:
- Neurogenetics, 2019, v. 20, n. 4, p. 197, doi. 10.1007/s10048-019-00584-3
- By:
- Publication type:
- Article
6
Extensive clinical and genetic workup is worthwhile in patients with Leigh-like syndrome due to the TSFM variant c.547G>A.
- Published in:
- 2019
- By:
- Publication type:
- Letter
7
Homozygous frameshift variant in NTNG2, encoding a synaptic cell adhesion molecule, in individuals with developmental delay, hypotonia, and autistic features.
- Published in:
- Neurogenetics, 2019, v. 20, n. 4, p. 209, doi. 10.1007/s10048-019-00583-4
- By:
- Publication type:
- Article