Journal article
Use of ultra-rapid whole-exome sequencing to diagnose congenital central hypoventilation syndrome
Shivanthan Shanthikumar, Ajay Kevat, Rachel Stapleton, Sebastian Lunke, Zornitza Stark, Moya Vandeleur
Pediatric Pulmonology | WILEY | Published : 2020
DOI: 10.1002/ppul.24686
Grants
Funding Acknowledgements
The authors would like to acknowledge the Royal Children's Hospital Foundation for funding the rapid genomic diagnosis program.