Exome sequencing is a valuable approach in critically ill patients with suspected monogenic disease: Diagnosis of X-linked centronuclear myopathy in preterm twins

Title
Exome sequencing is a valuable approach in critically ill patients with suspected monogenic disease: Diagnosis of X-linked centronuclear myopathy in preterm twins
Authors
Keywords
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Journal
Pediatrics and Neonatology
Volume 58, Issue 5, Pages 458-459
Publisher
Elsevier BV
Online
2016-11-22
DOI
10.1016/j.pedneo.2016.05.007

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