CFTR gene therapy, a method to rescue lung hypoplasia in congenital diaphragmatic hernia?
2006
despite progress in neonatal care and despite changing concepts in treatment in the recent years, the mortality rate of infants with congenital diaphragmatic hernia (CDH) remains high ([20][1]). Pulmonary hypoplasia and vascular alterations associated with CDH have tremendous postnatal functional
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