Exome sequencing is a valuable approach in critically ill patients with suspected monogenic disease: Diagnosis of X-linked centronuclear myopathy in preterm twins
Pediatr Neonatol. 2017 Oct;58(5):458-459.
doi: 10.1016/j.pedneo.2016.05.007.
Epub 2016 Nov 22.
1 Department of Pediatrics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany. Electronic address: j.johannsen@uke.de.
2 Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
3 Department of Pediatrics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
4 Institute of Human Genetics, Helmholtz Zentrum München, Neuherberg, Germany; Institute of Human Genetics, Technische Universität München, München, Germany.