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Hereditary xanthinuria type II associated with mental delay, autism, cortical renal cysts, nephrocalcinosis, osteopenia, and hair and teeth defects
  1. 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
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Citation

Zannolli R, Micheli V, Mazzei MA, et al
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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