Activation of cryptic splice sites is a frequent splicing defect mechanism caused by mutations in exon and intron sequences of the OPA1 gene. [electronic resource]

By: Contributor(s): Producer: 20070309Description: 767-71 p. digitalISSN:
  • 0340-6717
Subject(s): Online resources: In: Human genetics vol. 118
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't

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