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Mitochondrial genetics
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Complex I deficiency: clinical features, biochemistry and molecular genetics
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Authors

  • Elisa Fassone 1Mitochondrial Research Group, Clinical and Molecular Genetics Unit, UCL Institute of Child Health, London, UK PubMed articlesGoogle scholar articles
  • Shamima Rahman 1Mitochondrial Research Group, Clinical and Molecular Genetics Unit, UCL Institute of Child Health, London, UK2Metabolic Unit, Great Ormond Street Hospital, London, UK3MRC Centre for Neuromuscular Diseases, National Hospital for Neurology, London, UK PubMed articlesGoogle scholar articles
  1. Correspondence to Dr Shamima Rahman, Clinical and Molecular Genetics Unit, UCL Institute of Child Health, 30 Guilford Street, London WC1N 1EH, UK; shamima.rahman{at}ucl.ac.uk
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Citation

Fassone E, Rahman S
Complex I deficiency: clinical features, biochemistry and molecular genetics
Journal of Medical Genetics 2012;49:578-590.

Publication history

  • Received July 6, 2012
  • Accepted July 28, 2012
  • First published September 11, 2012.
Online issue publication 
October 06, 2016

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