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Neurology. Genetics|August 4, 2021
Mutation in ZDHHC15 Leads to Hypotonic Cerebral Palsy, Autism, Epilepsy, and Intellectual DisabilitySara A Lewis, Somayeh Bakhtiari, Jennifer Heim, et al.Neurology. Genetics|November 23, 2016
De novo FGF12 mutation in 2 patients with neonatal-onset epilepsyIlaria Guella, Linda Huh, Marna B McKenzie, et al.Neurology. Genetics|December 14, 2016
Clinical and genetic study of hereditary spastic paraplegia in CanadaNicolas Chrestian, Nicolas Dupré, Ziv Gan-Or, et al.Neurology. Genetics|March 31, 2017
GNAO1 encephalopathy: Broadening the phenotype and evaluating treatment and outcomeFederica Rachele Danti, Serena Galosi, Marta Romani, et al.Neurology. Genetics|February 10, 2017
Precision therapy for a new disorder of AMPA receptor recycling due to mutations in ATAD1Rebecca C Ahrens-Nicklas, George K E Umanah, Neal Sondheimer, et al.Neurology. Genetics|February 12, 2021
Erratum: Genetic Risk Scores and Hallucinations in Parkinson Disease PatientsNeurology. Genetics|December 22, 2021
TNNI1 Mutated in Autosomal Dominant Proximal ArthrogryposisYukako Nishimori, Aritoshi Iida, Masashi Ogasawara, et al.Neurology. Genetics|October 27, 2022
Investigating Late-Onset Pompe Prevalence in Neuromuscular Medicine Academic Practices: The IPaNeMA StudyMarie Wencel, Aziz Shaibani, Namita A Goyal, et al.Neurology. Genetics|September 12, 2022
Alanyl-tRNA Synthetase 1 Gene Variants in Hereditary Neuropathy: Genotype and Phenotype OverviewSigne Setlere, Marija Jurcenko, Linda Gailite, et al.Pageof 87