A case of congenital central hypoventilation syndrome with PHOX2B gene mutation in a Korean neonate. [electronic resource]

By: Contributor(s): Producer: 20101124Description: 1237-40 p. digitalISSN:
  • 1598-6357
Subject(s): Online resources: In: Journal of Korean medical science vol. 25
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Publication Type: Case Reports; Journal Article

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