Clinical features and natural history of neuroferritinopathy caused by the FTL1 460InsA mutation (2007)

Author(s): Chinnery PF, Crompton DE, Birchall D, Jackson MJ, Coulthard A, Lombes A, Quinn N, Wills A, Fletcher N, Mottershead JP, Cooper P, Kellett M, Bates D, Burn J

      • Journal: Brain
      • Volume: 130
      • Issue: 1
      • Pages: 110-119
      • Publisher: Oxford University
      • Publication type: Article
      • Bibliographic status: Published

      Professor Sir John Burn
      Professor of Clinical Genetics