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A phenocopy of CAII deficiency: a novel genetic explanation for inherited infantile osteopetrosis with distal renal tubular acidosis
- 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
Citation
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
April 27, 2016
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Copyright 2003 Journal of Medical Genetics