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Publication:

The clinical spectrum of the m.10191T > C mutation in complex I-deficient Leigh syndrome (2012)

Author(s): Nesbitt V, Morrison PJ, Crushell E, Donnelly DE, Alston CL, He LP, Mcfarland R, Taylor RW

      • Date: 27-02-2012
      • Journal: Developmental Medicine and Child Neurology
      • Volume: 54
      • Issue: 6
      • Pages: 500-506
      • Publication type: Review
      • Bibliographic status: Published

      Keywords: MITOCHONDRIAL-DNA MUTATIONS ND3 GENE MISSENSE MUTATION DISEASE CHILDREN ENCEPHALOPATHY DISORDERS FAMILIES

      Staff

      Charlotte Alston
      Associate Researcher

      Dr Bobby McFarland
      Clinical Senior Lecturer and Hon Consultant Paediatric Neurologist

      Professor Robert Taylor
      Professor of Mitochondrial Pathology