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Original article
Mutations in MYO1H cause a recessive form of central hypoventilation with autonomic dysfunction
- Correspondence to Stefan Mundlos, Max-Planck-Institute for Molecular Genetics, Ihnestraße 63-73, 14195 Berlin, Germany ; mundlos{at}molgen.mpg.de
Citation
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.
Online issue publication
February 28, 2018
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© Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2017. All rights reserved. No commercial use is permitted unless otherwise expressly granted.