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Electronic letters
Hereditary xanthinuria type II associated with mental delay, autism, cortical renal cysts, nephrocalcinosis, osteopenia, and hair and teeth defects
- Correspondence to: Raffaella Zannolli MD, Department of Pediatrics, Obstetrics and Reproductive Medicine, Section of Pediatrics, Policlinico Le Scotte, University of Siena, Siena, Italy; zannolliunisi.it
Citation
Hereditary xanthinuria type II associated with mental delay, autism, cortical renal cysts, nephrocalcinosis, osteopenia, and hair and teeth defects
Publication history
- First published November 19, 2003.
Online issue publication
November 19, 2003
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Copyright 2003 Journal of Medical Genetics