Association studies in genetics

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Predictive role of heterozygous p.R4810K of RNF213 in the phenotype of Chinese moyamoya disease
Yue Wang, Zhengshan Zhang, Ling Wei, et al.

Neurology January 16, 2020
Article
Analysis of common and rare VPS13C variants in late-onset Parkinson disease
Uladzislau Rudakou, Jennifer A. Ruskey, Lynne Krohn, et al.

Neurology Genetics January 09, 2020
Article
Analysis of FUS, PFN2, TDP-43, and PLS3 as potential disease severity modifiers in spinal muscular atrophy
Renske I. Wadman, Marc D. Jansen, Chantall A.D. Curial, et al.

Neurology Genetics January 03, 2020
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HSAN-VIA spectrum disorder based on dystonin isoform expression
Anisha Lynch-Godrei, Rashmi Kothary

Neurology Genetics January 02, 2020