Two novel mutations of the gene for Kir 1.1 (ROMK) in neonatal Bartter syndrome. [electronic resource]

By: Contributor(s): Producer: 19980424Description: 69-71 p. digitalISSN:
  • 0931-041X
Subject(s): Online resources: In: Pediatric nephrology (Berlin, Germany) vol. 12
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't

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