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Neurology. Genetics|January 16, 2023
Prevalence of Frontotemporal Dementia in Females of 5 Hispanic Families With R159H VCP Multisystem ProteinopathyAlyaa Shmara, Liliane Gibbs, Ryan Patrick Mahoney, et al.
Neurology. Genetics|November 20, 2019
Homozygous pathogenic variant in BRAT1 associated with nonprogressive cerebellar ataxiaAreej Mahjoub, Zuzana Cihlarova, Martine Tétreault, et al.
Neurology. Genetics|July 8, 2021
Erratum: KCNQ2 Encephalopathy Manifesting With Rett-like Features: A Follow-up Into Adulthood
Neurology. Genetics|October 5, 2018
Protein network analysis reveals selectively vulnerable regions and biological processes in FTDLuke W Bonham, Natasha Z R Steele, Celeste M Karch, et al.
Neurology. Genetics|May 25, 2019
Lithium chloride corrects weakness and myopathology in a preclinical model of LGMD1DAndrew R Findlay, Rocio Bengoechea, Sara K Pittman, et al.
Neurology. Genetics|May 2, 2019
Clinical, genetic, and pathologic characterization of FKRP Mexican founder mutation c.1387A>GAngela J Lee, Karra A Jones, Russell J Butterfield, et al.
Neurology. Genetics|May 2, 2019
Somatic expansion of the C9orf72 hexanucleotide repeat does not occur in ALS spinal cord tissuesJay P Ross, Claire S Leblond, Hélène Catoire, et al.
Neurology. Genetics|May 27, 2022
Erratum: Multigene Panel Testing in a Large Cohort of Adults With Epilepsy: Diagnostic Yield and Clinically Actionable Genetic Findings
Neurology. Genetics|May 27, 2022
Clinical Evidence for Variegated Silencing in Patients With Friedreich AtaxiaLayne N Rodden, Christian Rummey, Yi Na Dong, et al.
Neurology. Genetics|May 27, 2022
Erratum: Migraine, Stroke, and Cervical Arterial Dissection: Shared Genetics for a Triad of Brain Disorders With Vascular Involvement
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