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Neurology. Genetics|April 29, 2016
New susceptible variant of COQ2 gene in Japanese patients with sporadic multiple system atrophyZhuoran Sun, Yasuyuki Ohta, Toru Yamashita, et al.Neurology. Genetics|April 29, 2016
Familial aggregation of Parkinson disease in Utah: A population-based analysis using death certificatesRodolfo Savica, Lisa A Cannon-Albright, Stefan PulstNeurology. Genetics|April 29, 2016
Paroxysmal hypnogenic dyskinesia is associated with mutations in the PRRT2 geneXiao-Rong Liu, Dan Huang, Jie Wang, et al.Neurology. Genetics|April 29, 2016
Deleterious mutation in GPR88 is associated with chorea, speech delay, and learning disabilitiesFadi Alkufri, Avraham Shaag, Bassam Abu-Libdeh, et al.Neurology. Genetics|April 29, 2016
Clinical and genetic features of cervical dystonia in a large multicenter cohortMark S LeDoux, Satya R Vemula, Jianfeng Xiao, et al.Neurology. Genetics|April 29, 2016
DNA variants in CACNA1C modify Parkinson disease risk only when vitamin D level is deficientLiyong Wang, Lizmarie Maldonado, Gary W Beecham, et al.Neurology. Genetics|May 17, 2016
Genomic mechanisms underlying PARK2 large deletions identified in a cohort of patients with PDSara Morais, Rita Bastos-Ferreira, Jorge Sequeiros, et al.Neurology. Genetics|April 12, 2016
Turkish families with juvenile motor neuron disease broaden the phenotypic spectrum of SPG11Ceren Iskender, Ece Kartal, Fulya Akcimen, et al.Neurology. Genetics|April 12, 2016
Spinocerebellar ataxia type 10 in Chinese HanKang Wang, Karen N McFarland, Jilin Liu, et al.Neurology. Genetics|April 12, 2016
Clinical and imaging findings in Parkinson disease associated with the A53E SNCA mutationMika H Martikainen, Markku Päivärinta, Marja Hietala, et al.Pageof 86