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Mosaic de novo SNRPN gene variant associated with Prader-Willi syndrome

Authors

  1. Correspondence to Dr Pedro A Sanchez-Lara, Department of Pediatrics, Cedars-Sinai Medical Center, Los Angeles, CA 90048, USA; Pedro.Sanchez{at}cshs.org
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Citation

Huang Y, Grand K, Kimonis V, et al
Mosaic de novo SNRPN gene variant associated with Prader-Willi syndrome

Publication history

  • Received December 28, 2020
  • Accepted May 11, 2021
  • First published June 7, 2021.

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