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Neurology. Genetics|February 12, 2020
Psychometric properties of the Friedreich Ataxia Rating ScaleChristian Rummey, Louise A Corben, Martin B Delatycki, et al.
Neurology. Genetics|February 12, 2020
Analysis of FUS, PFN2, TDP-43, and PLS3 as potential disease severity modifiers in spinal muscular atrophyRenske I Wadman, Marc D Jansen, Chantall A D Curial, et al.
Neurology. Genetics|February 12, 2020
COL4A1-related autosomal recessive encephalopathy in 2 Turkish childrenAhmet Yaramis, Hanns Lochmüller, Ana Töpf, et al.
Neurology. Genetics|February 12, 2020
Delineating MT-ATP6-associated disease: From isolated neuropathy to early onset neurodegenerationClaudia Stendel, Christiane Neuhofer, Elisa Floride, et al.
Neurology. Genetics|August 18, 2020
Hydrocephalus and diffuse choroid plexus hyperplasia in primary ciliary dyskinesia-related MCIDAS mutationEvie Alexandra Robson, Luke Dixon, Liam Causon, et al.
Neurology. Genetics|August 18, 2020
D-DEMØ, a distinct phenotype caused by ATP1A3 mutationsLyndsey Prange, Milton Pratt, Kristin Herman, et al.
Neurology. Genetics|July 9, 2020
Brainstem ischemic syndrome in juvenile NF2John W Henson, Tara Benkers, Connor McCormick
Neurology. Genetics|July 9, 2020
Synonymous variants associated with Alzheimer disease in multiplex familiesMin Tang, Maria Eugenia Alaniz, Daniel Felsky, et al.
Neurology. Genetics|August 6, 2020
APOE ϵ4 modifies the relationship between infectious burden and poor cognitionChen Zhao, Kevin Strobino, Yeseon Park Moon, et al.
Neurology. Genetics|August 6, 2020
Disease-modifying effects of an SCAF4 structural variant in a predominantly SOD1 ALS cohortJulia Pytte, Loren L Flynn, Ryan S Anderton, et al.
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