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Original Article
Mutations in MYO1H cause a recessive form of central hypoventilation with autonomic dysfunction

Authors

  1. Correspondence to Stefan Mundlos, Max-Planck-Institute for Molecular Genetics, Ihnestraße 63-73, 14195 Berlin, Germany ; mundlos{at}molgen.mpg.de
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Citation

Spielmann M, Hernandez-Miranda LR, Ceccherini I, et al
Mutations in MYO1H cause a recessive form of central hypoventilation with autonomic dysfunction

Publication history

  • Received April 26, 2017
  • Revised June 14, 2017
  • Accepted June 16, 2017
  • First published August 4, 2017.

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