Article info
Case report
Recurrent apnoea and respiratory failure in an infant: congenital central hypoventilation syndrome with a novel PHOX2B gene variant
- Correspondence to Dr Ajay S Kasi; ajay.kasi{at}emory.edu
Citation
Recurrent apnoea and respiratory failure in an infant: congenital central hypoventilation syndrome with a novel PHOX2B gene variant
Publication history
- Accepted March 5, 2021
- First published March 19, 2021.
Online issue publication
January 24, 2024
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Copyright information
© BMJ Publishing Group Limited 2021. No commercial re-use. See rights and permissions. Published by BMJ.