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Neurology. Genetics|November 11, 2016
Novel HSPB1 mutation causes both motor neuronopathy and distal myopathyD J Lewis-Smith, J Duff, A Pyle, et al.Neurology. Genetics|November 11, 2016
Germline and somatic mutations in the MTOR gene in focal cortical dysplasia and epilepsyRikke S Møller, Sarah Weckhuysen, Mathilde Chipaux, et al.Neurology. Genetics|November 24, 2016
Phenotypic convergence of Menkes and Wilson diseaseBoglarka Bansagi, David Lewis-Smith, Endre Pal, et al.Neurology. Genetics|March 8, 2019
Copy number variation of LINGO1 in familial dystonic tremorVafa Alakbarzade, Thomas Iype, Barry A Chioza, et al.Neurology. Genetics|July 20, 2019
Human GABRG2 generalized epilepsy: Increased somatosensory and striatothalamic connectivityMangor Pedersen, Magdalena Kowalczyk, Amir Omidvarnia, et al.Neurology. Genetics|January 19, 2017
ABCA7 loss-of-function variants, expression, and neurologic disease riskMariet Allen, Sarah J Lincoln, Morgane Corda, et al.Neurology. Genetics|March 16, 2017
Research conference summary from the 2014 International Task Force on ATP1A3-Related DisordersHendrik Rosewich, Matthew T Sweney, Suzanne DeBrosse, et al.Neurology. Genetics|September 14, 2019
Next-generation sequencing approach to hyperCKemia: A 2-year cohort studyAnna Rubegni, Alessandro Malandrini, Claudia Dosi, et al.Neurology. Genetics|September 14, 2019
Impaired kidney structure and function in spinal muscular atrophyFlávia C Nery, Jennifer J Siranosian, Ivy Rosales, et al.Neurology. Genetics|August 20, 2016
A new dawn for genetic association studies in multiple sclerosisOrhun H KantarciPageof 86