PPP1R21 homozygous null variants associated with developmental delay, muscle weakness, distinctive facial features, and brain abnormalities. [electronic resource]

By: Contributor(s): Producer: 20191028Description: 351-355 p. digitalISSN:
  • 1399-0004
Subject(s): Online resources: In: Clinical genetics vol. 94
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Publication Type: Case Reports; Journal Article

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