Motor neuron diseases caused by a novel VRK1 variant - A genotype/phenotype study.
Maryam SedghiAli-Reza MoslemiMontse OliveMasoud EtemadifarBehnaz AnsariJafar NasiriLeila EmrahiHamid-Reza MianesazNigel G LaingHoma TajsharghiPublished in: Annals of clinical and translational neurology (2019)
Our findings unveil the impact of the variant on the VRK1 transcript and further support the implication of VRK1 in the pathogenesis of lower motor neuron diseases.
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