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Two patients with MIRAGE syndrome lacking haematological features: role of somatic second-site reversion SAMD9 mutations

Authors

  1. Correspondence to Dr Satoshi Narumi, Department of Molecular Endocrinology, National Research Institute for Child Health and Development, Setagaya-ku, Tokyo 157-8535, Japan; narumi-s{at}ncchd.go.jp
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Citation

Shima H, Koehler K, Nomura Y, et al
Two patients with MIRAGE syndrome lacking haematological features: role of somatic second-site reversion SAMD9 mutations

Publication history

  • Received 5 September 2017
  • Revised 24 October 2017
  • Accepted 29 October 2017
  • Published online 24 November 2017.

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