The frequency of the m.1555A > G (MTRNR1) variant in UK patients with suspected mitochondrial deafness

Peter KullarMitochondrial Biology Unit, Cambridge Biomedical, Campus, Hills Road, Cambridge, UK, Correspondence[email protected]

Patrick F. ChinneryMitochondrial Biology Unit, Cambridge Biomedical, Campus, Hills Road, Cambridge, UK,

Charlotte L. AlstonWellcome Trust Centre for Mitochondrial Research, Institute of Neuroscience, Newcastle University, Newcastle upon Tyne, UK,

Emma L. BlakelyWellcome Trust Centre for Mitochondrial Research, Institute of Neuroscience, Newcastle University, Newcastle upon Tyne, UK,

Robert W. TaylorWellcome Trust Centre for Mitochondrial Research, Institute of Neuroscience, Newcastle University, Newcastle upon Tyne, UK,

Sarah BallMicropathology Ltd, University of Warwick Science Park, Venture Centre, Coventry, UK,

Ann-Marie DifferDepartment of Molecular Genetics, Great Ormond Street for Children NHS Trust and UCL Institute of Child Health, London, UK,

Carl FratterOxford Medical Genetics Laboratories, Oxford University Hospitals NHS Trust, Oxford, UK,

Mary G. SweeneyNeurogenetics Unit, National Hospital for Neurology and Neurosurgery, London, UK

References