Low-density oligonucleotide microarrays - A major step in Wilson's disease diagnosis.

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    • Abstract:
      The article discusses various studies which showed the ineffectiveness of screening individuals in India for one major founder mutation to detect Wilson's disease (WD), a monogenic disorder of copper accumulation due to mutation in the copper transporting ATPase gene. Topics discussed include the advantage of the genetic diagnosis of WD and low-density microarray for WD detection.