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neurogenetics
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Volume 20, Issue 4, October 2019
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1. Nervous NDRGs: the N-myc downstream–regulated gene family in the central and peripheral nervous system
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Simone L. Schonkeren, Maartje Massen, Raisa van der Horst, Alexander Koch.
2. VPS53 gene is associated with a new phenotype of complicated hereditary spastic paraparesis
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Moran Hausman-Kedem, Shay Ben-Shachar, Shay Menascu, Karen Geva.
3. Identification and characterization of novel and rare susceptible variants in Indian amyotrophic lateral sclerosis patients
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Priyam Narain, Aditya K. Padhi, Upma Dave, Dibyakanti Mishra, Rohit Bhatia.
4. Homozygous frameshift variant in NTNG2, encoding a synaptic cell adhesion molecule, in individuals with developmental delay, hypotonia, and autistic features
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Bassam Abu-Libdeh, Motee Ashhab, Maher Shahrour, Muhannad Daana.
5. Frequency of the LRRK2 G2019S mutation in South African patients with Parkinson’s disease
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Nicola du Toit, Riaan van Coller, David G. Anderson, Jonathan Carr.
6. Extensive clinical and genetic workup is worthwhile in patients with Leigh-like syndrome due to the TSFM variant c.547G>A
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Josef Finsterer.
7. Acknowledgement to referees 2018/2019
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