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Neurology. Genetics|April 29, 2016
Exonic deletion of SLC9A9 in autism with epilepsyMeeta Cardon, Karen D Evankovich, J Lloyd HolderNeurology. Genetics|April 29, 2016
Copy number variants in absence epilepsy: Further complications of the pictureChantal DepondtNeurology. Genetics|April 29, 2016
Parkinson disease (PARK) genes are somatically mutated in cutaneous melanomaRivka Inzelberg, Yardena Samuels, Esther Azizi, et al.Neurology. Genetics|April 12, 2016
Mutation in PNKP presenting initially as axonal Charcot-Marie-Tooth diseaseJosé Luiz Pedroso, Clarissa R R Rocha, Lucia I Macedo-Souza, et al.Neurology. Genetics|April 12, 2016
Novel GABRG2 mutations cause familial febrile seizuresMorgane Boillot, Mélanie Morin-Brureau, Fabienne Picard, et al.Neurology. Genetics|April 12, 2016
Genetic profile for suspected dysferlinopathy identified by targeted next-generation sequencingRumiko Izumi, Tetsuya Niihori, Toshiaki Takahashi, et al.Neurology. Genetics|April 12, 2016
Polyneuropathy in a young Belgian patient: A novel heterozygous mutation in the WNK1/HSN2 geneJeroen de Filette, Danielle Hasaerts, Sara Seneca, et al.Neurology. Genetics|April 12, 2016
Overlap between Parkinson disease and Alzheimer disease in ABCA7 functional variantsKaren Nuytemans, Lizmarie Maldonado, Aleena Ali, et al.Neurology. Genetics|April 12, 2016
In silico prioritization based on coexpression can aid epileptic encephalopathy gene discoveryKaren L Oliver, Vesna Lukic, Saskia Freytag, et al.Pageof 86