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Hereditary C1q deficiency and secondary Sjögren’s syndrome
  1. Correspondence to:
    Dr E P A H Hoppenreijs
    Department of Paediatrics, University Medical Centre Utrecht, Wilhelmina Kinderziekenhuis, PO Box 85090, 3508 AB Utrecht, the Netherlands; e.p.a.h.hoppenreijswkz.azu.nl
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Citation

Hoppenreijs EPAH, van Dijken PJ, Kabel PJ, et al
Hereditary C1q deficiency and secondary Sjögren’s syndrome

Publication history

  • Accepted December 22, 2003
  • First published October 12, 2004.
Online issue publication 
April 13, 2016

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