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Low-density oligonucleotide microarrays - A major step in Wilson's disease diagnosis.
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- Author(s): Gupta, Arnab1
- Source:
Indian Journal of Medical Research. Feb2015, Vol. 141 Issue 2, p145-147. 3p.
- Subject Terms:
- Additional Information
- 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.
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