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

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"The frequency of the m.1555A > G (MTRNR1) variant in UK patients with suspected mitochondrial deafness." Hearing, Balance and Communication, 14(2), pp. 101–102

Disclosure statement

The authors declare no conflict of interests.

Funding information

RWT is supported by the Wellcome Trust Centre for Mitochondrial Research, the Medical Research Council (UK) Centre for Translational Muscle Disease Research, The Lily Foundation and the UK NHS Highly Specialised Commissioners which funds the ‘Rare Mitochondrial Disorders of Adults and Children’ Diagnostic Service in Newcastle upon Tyne (http://www.newcastle-mitochondria.com). CLA is a recipient of a National Institute for Health Research (NIHR) doctoral fellowship. The views expressed are those of the authors and not necessarily those of the NHS, the NIHR or the Department of Health. PK and PFC are supported by the Wellcome Trust Centre for Mitochondrial Research.

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

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

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