Associated Papers
The phenotyping dilemma in VRK1-related motor neuron disease: a Turkish family with young-onset amyotrophic lateral sclerosis caused by a novel mutation.
Mercan M et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration, 2025
CMT2 and distal hereditary motor neuropathy associated with VRK1 variants: Case series.
Živković SA et al.
Neuromuscular Disorders : Nmd, 2025
Pathogenic effects of Leu200Pro and Arg387His VRK1 protein variants on phosphorylation targets and H4K16 acetylation in distal hereditary motor neuropathy.
Campos-Díaz A et al.
Journal of Molecular Medicine (berlin, Germany), 2024
Adult-Onset Spinal Muscular Atrophy due to Mutations in the VRK1 Gene.
Sung A et al.
Neurology. Genetics, 2021
VRK1 variants in two Portuguese unrelated patients with childhood-onset motor neuron disease.
Silva DP et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration, 2020
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