The clinical spectrum of mitochondrial genetic disorders
Alan Fryer, Ruth Newbury-Ecob, Matthew A Kirkman, Patrick Yu-Wai-Man and Patrick F Chinnery Joint Committee on Medical Genetics (Royal College of Physicians, Royal College of Pathologists, British Society of Human Genetics)
DOI: https://doi.org/10.7861/clinmedicine.8-6-601
Clin Med December 2008 Alan Fryer
Royal Liverpool Children's Hospital
MB FRCPRoles: Consultant Clinical Geneticist
Ruth Newbury-Ecob
St Michaels Hospital, Bristol
FRCP FRCPCH MDRoles: Consultant in Clinical Genetics
Matthew A Kirkman
Mitochondrial Research Group, The Medical School, Newcastle University
BScRoles: Medical student
Patrick Yu-Wai-Man
Mitochondrial Research Group, The Medical School, Newcastle University
BMedSci MRCOphthRoles: Specialist Registrar in Ophthalmology and MRC Clinical Research Fellow
Patrick F Chinnery
Mitochondrial Research Group, The Medical School, Newcastle University
BMedSci PhD FRCPath FRCPRoles: Professor of Neurogenetics, Consultant Neurologist and Wellcome Trust Senior Fellow in Clinical Science
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vol. 8 no. 6 601-606
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© 2008 Royal College of Physicians
Other Contributors:
- Alan Fryer [MB FRCP], Consultant Clinical Geneticist, Royal Liverpool Children's Hospital
- Ruth Newbury-Ecob [FRCP FRCPCH MD], Consultant in Clinical Genetics, St Michaels Hospital, Bristol
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The clinical spectrum of mitochondrial genetic disorders
Matthew A Kirkman, Patrick Yu-Wai-Man, Patrick F Chinnery
Clinical Medicine Dec 2008, 8 (6) 601-606; DOI: 10.7861/clinmedicine.8-6-601
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