#
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

      Dr Bobby McFarland
      DoH/HEFCE Clinical Senior Lecturer and Consultant Paediatric Neurologist

      Professor Robert Taylor
      Professor of Mitochondrial Pathology