event Whole genome sequencing in ophthalmoplegic myasthenia gravis: a hypothesis-generating analysis to assess a rare phenotype 15 November 2018
15 November 2018 Postgraduate seminar room 2 Level 2, Barnard Fuller Building Faculty of Health Sciences neuroscience@uct.ac.za Whole genome sequencing in ophthalmoplegic myasthenia gravis: a hypothesis-generating analysis to assess a rare phenotype Dr Melissa Nel, Division of Neurology
