Clinical phenotype of an Italian family with a new mutation in the PRPF8 gene. [electronic resource]

By: Contributor(s): Producer: 20070116Description: 779-81 p. digitalISSN:
  • 1120-6721
Subject(s): Online resources: In: European journal of ophthalmology vol. 16
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

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