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  • 4193delC, a common mutation causing Wilson’s disease in Saudi Arabia: rapid molecular screening of patients and carriers

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4193delC, a common mutation causing Wilson’s disease in Saudi Arabia: rapid molecular screening of patients and carriers
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Authors

  1. Correspondence to:
 Dr R Majumdar, Department of Medicine (mail code 1443), King Fahad National Guard Hospital, Riyadh 11426, Saudi Arabia;
 ramanathm{at}hotmail.com
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Citation

Majumdar R, Al Jumah M, Fraser M
4193delC, a common mutation causing Wilson’s disease in Saudi Arabia: rapid molecular screening of patients and carriers
Molecular Pathology 2003;56:302-304.

Publication history

  • Accepted June 20, 2003
  • First published September 26, 2003.
Online issue publication 
September 26, 2003

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Copyright 2003 Journal of Clinical Pathology