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Neurology. Genetics|March 19, 2020
Heritability of cervical spinal cord structureLinda Solstrand Dahlberg, Olivia Viessmann, Clas LinnmanNeurology. Genetics|March 27, 2020
Heterozygous STUB1 missense variants cause ataxia, cognitive decline, and STUB1 mislocalizationDong-Hui Chen, Caitlin Latimer, Mayumi Yagi, et al.Neurology. Genetics|August 28, 2020
Variant repeats within the DMPK CTG expansion protect function in myotonic dystrophy type 1Jacob N Miller, Ellen van der Plas, Mark Hamilton, et al.Neurology. Genetics|December 28, 2018
Erratum: Confirming TDP2 mutation in spinocerebellar ataxia autosomal recessive 23 (SCAR23)Neurology. Genetics|November 23, 2020
Late-onset vs nonmendelian early-onset Alzheimer disease: A distinction without a difference?Christiane Reitz, Ekaterina Rogaeva, Gary W BeechamNeurology. Genetics|July 11, 2022
FUS-P525L Juvenile Amyotrophic Lateral Sclerosis and Intellectual Disability: Evidence for Association and Oligogenic InheritanceOrly Goldstein, Talya Inbar, Merav Kedmi, et al.Neurology. Genetics|April 12, 2016
Genetic analysis for a shared biological basis between migraine and coronary artery diseaseBendik S Winsvold, Christopher P Nelson, Rainer Malik, et al.Neurology. Genetics|April 12, 2016
PFKM gene defect and glycogen storage disease GSDVII with misleading enzyme histochemistryMari Auranen, Johanna Palmio, Emil Ylikallio, et al.Neurology. Genetics|April 12, 2016
A novel DYNC1H1 mutation causing spinal muscular atrophy with lower extremity predominanceQi Niu, Xingxia Wang, Mingchao Shi, et al.Pageof 88