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Neurology. Genetics|August 10, 2023
Genome-wide Analysis of Motor Progression in Parkinson DiseaseAlejandro Martínez Carrasco, Raquel Real, Michael Lawton, et al.
Neurology. Genetics|April 15, 2024
Clinical, Neuroimaging, and Metabolic Footprint of the Neurodevelopmental Disorder Caused by Monoallelic HK1 VariantsSaskia B Wortmann, Rene G Feichtinger, Lucia Abela, et al.
Neurology. Genetics|May 8, 2024
APOE ε4 Allele Frequency Among Cognitively Healthy Members of an Ojibwe Tribal NationAdam D Block, Madelyn R Castro, Adam Hansen, et al.
Neurology. Genetics|May 8, 2024
A Novel TSC2 c.2489T>C Missense Variant Associated With Tuberous Sclerosis Complex: Case ReportYujie Lai, Yuanye Ma, Biao Luo, et al.
Neurology. Genetics|April 30, 2024
Two Novel Variants in PI4KA in a Family Presenting With Hereditary Spastic Paraparesis: A Case ReportJevin M Parmar, Elyshia L McNamara, Phillipa J Lamont, et al.
Neurology. Genetics|June 22, 2026
Erratum: NNZ-2591 in Children and Adolescents With Phelan-McDermid Syndrome: Single-Group, Open-Label, Phase 2 Trial ResultsAnn M Neumeyer, Siddharth Srivastava, J Lloyd Holder, et al.
Neurology. Genetics|July 11, 2022
Novel TOP3A Variant Associated With Mitochondrial Disease: Expanding the Clinical Spectrum of Topoisomerase III Alpha-Related DiseasesGuido Primiano, Alessandra Torraco, Daniela Verrigni, et al.
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