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An atypical case of hypoxanthine-guanine phosphoribosyltransferase deficiency (Lesch-Nyhan syndrome) : I. Clinical studies

✍ Scribed by R. A. Geerdink; W. H. M. de Vries; J. Willemse; T. L. Oei; C. H. M. M. de Bruyn

No coin nor oath required. For personal study only.

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