Genetic dysfunction of <i>MT-ATP6</i> causes axonal Charcot-Marie-Tooth disease
Robert D. S. Pitceathly(National Hospital for Neurology and Neurosurgery), Michael G. Hanna(National Hospital for Neurology and Neurosurgery), Michael R. Rose(University of Oxford), Carol A. Crowe(Cleveland Clinic), Ellen Cottenie(UCL Australia), Mary M. Reilly(National Hospital for Neurology and Neurosurgery), Cheryl Longman, Ese Mudanohwo(University College London), Rupert Page(Poole Hospital NHS Foundation Trust), Shamima Rahman(Great Ormond Street Hospital for Children NHS Foundation Trust), Janice L. Holton(National Hospital for Neurology and Neurosurgery), Sinéad M. Murphy(Trinity College Dublin), Michael P. Lunn(UCL Biomedical Research Centre), Frances Flinter(Guy's and St Thomas' NHS Foundation Trust), Henry Houlden(Queen Mary University of London), Annapurna Chalasani(UCL Australia), Michael Champion, Jacqueline Palace(John Radcliffe Hospital), Iain P. Hargreaves(Liverpool John Moores University), John M. Land(UCL Australia), Cathy E. Woodward(University College London), Simon Heales(UCL Australia), Mary G. Sweeney(Cedars-Sinai Medical Center), Julian Blake(Norfolk and Norwich University Hospitals NHS Foundation Trust), S. Robb(University College London)
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