A recurrent large Alu-mediated deletion in the hypoxanthine phosphoribosyltransferase (HPRT1) gene associated with Lesch-Nyhan syndrome

Makiko Mizunuma, Shin Fujimori, Hitoshi Ogino, Takamasa Ueno, Hirokazu Inoue, Naoyuki Kamatani
  • Human Mutation, January 2001, Wiley
  • DOI: 10.1002/humu.1214
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The following have contributed to this page: Dr Takamasa Ueno

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