Relevance of SOX17 variants for hypomyelinating leukodystrophies and congenital anomalies of the kidney and urinary tract (CAKUT). [electronic resource]

By: Contributor(s): Producer: 20120629Description: 261-7 p. digitalISSN:
  • 1469-1809
Subject(s): Online resources: In: Annals of human genetics vol. 76
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't

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