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PDFOriginal article
Novel ATP6V1B1 and ATP6V0A4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing loss
- Correspondence to: Dr F E Karet, Departments of Medical Genetics and Nephrology, Cambridge Institute for Medical Research, Addenbrooke’s Hospital, Box 139, Cambridge CB2 2XY, UK; fek1000{at}cam.ac.uk
Citation
Novel ATP6V1B1 and ATP6V0A4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing loss
Publication history
- Accepted July 15, 2002
- Revised July 15, 2002
- First published November 1, 2002.
Online issue publication
November 01, 2002
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Copyright 2002 Journal of Medical Genetics