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A phenocopy of CAII deficiency: a novel genetic explanation for inherited infantile osteopetrosis with distal renal tubular acidosis
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  1. Correspondence to:
 Dr F E Karet, Cambridge Institute for Medical Research, Box 139, Addenbrooke’s Hospital, Cambridge CB2 2XY, UK;
 fek1000{at}cam.ac.uk
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Citation

Borthwick KJ, Kandemir N, Topaloglu R, et al
A phenocopy of CAII deficiency: a novel genetic explanation for inherited infantile osteopetrosis with distal renal tubular acidosis

Publication history

  • Accepted October 10, 2002
  • Revised October 9, 2002
  • First published February 1, 2003.
Online issue publication 
February 01, 2003

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