Comment on

• Haemolytic anaemia as a first sign of Wilson's disease.

  Balkema S, Hamaker ME, Visser HP, Heine GD, Beuers U. Balkema S, et al. Neth J Med. 2008 Sep;66(8):344-7. Neth J Med. 2008. PMID: 18809982
• Value of molecular analysis of Wilson's disease in the absence of tissue copper deposits: a novel ATP7B mutation in an adult patient.

  Kok KF, Hoevenaars B, Waanders E, Drenth JP. Kok KF, et al. Neth J Med. 2008 Sep;66(8):348-50. Neth J Med. 2008. PMID: 18809983