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Book Chapter

Molecular Analysis of Wilson Disease Gene in French Patients

  • Ceballos-Picot I
  • Nicole A
  • Aral B
  • et al.
Springer US, (2002), 917-921
DOI: 10.1007/0-306-47466-2_290
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Abstract

Wilson disease (WD) is an autosomal recessive disorder of copper transport resulting from toxic copper accumulation in liver and brain. Its clinical expression includes hepatic and/or neurological manifestations. The disease has a worldwide prevalence of 1 in 35,000 people …

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Ceballos-Picot, I., Nicole, A., Aral, B., Franvel, C., Soulié, C., Lassal, H., … Chappuis, P. (2002). Molecular Analysis of Wilson Disease Gene in French Patients. In Trace Elements in Man and Animals 10 (pp. 917–921). Springer US. https://doi.org/10.1007/0-306-47466-2_290

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