Nervous NDRGs: the N-myc downstream–regulated gene family in the central and peripheral nervous system Simone L. SchonkerenMaartje MassenVeerle Melotte Review Article Open access 04 September 2019 Pages: 173 - 186
VPS53 gene is associated with a new phenotype of complicated hereditary spastic paraparesis Moran Hausman-KedemShay Ben-ShacharAviva Fattal-Valevski Original Article 16 August 2019 Pages: 187 - 195
Identification and characterization of novel and rare susceptible variants in Indian amyotrophic lateral sclerosis patients Priyam NarainAditya K. PadhiJames Gomes Original Article 20 August 2019 Pages: 197 - 208
Homozygous frameshift variant in NTNG2, encoding a synaptic cell adhesion molecule, in individuals with developmental delay, hypotonia, and autistic features Bassam Abu-LibdehMotee AshhabTamar Harel Original Article 02 August 2019 Pages: 209 - 213
Frequency of the LRRK2 G2019S mutation in South African patients with Parkinson’s disease Nicola du ToitRiaan van CollerSoraya Bardien Short Communication 06 September 2019 Pages: 215 - 218
Extensive clinical and genetic workup is worthwhile in patients with Leigh-like syndrome due to the TSFM variant c.547G>A Josef Finsterer Letter to Editor 03 August 2019 Pages: 219 - 220