(Q35441188)
Statements
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Hereditary xanthinuria type II associated with mental delay, autism, cortical renal cysts, nephrocalcinosis, osteopenia, and hair and teeth defects (English)
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Zannolli R
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Micheli V
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Mazzei MA
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Sacco P
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Piomboni P
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Bruni E
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Miracco C
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de Santi MM
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Terrosi Vagnoli P
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Volterrani L
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Pellegrini L
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Livi W
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Lucani B
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Gonnelli S
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Burlina AB
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Jacomelli G
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Macucci F
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Pucci L
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Fimiani M
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Swift JA
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Zappella M
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Morgese G
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1 November 2003
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40
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11
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e121
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Identifiers
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