Structural model of the OPA1 GTPase domain may explain the molecular consequences of a novel mutation in a family with autosomal dominant optic atrophy. [electronic resource]

By: Contributor(s): Producer: 20061106Description: 702-6 p. digitalISSN:
  • 0014-4835
Subject(s): Online resources: In: Experimental eye research vol. 83
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Publication Type: Letter; Research Support, Non-U.S. Gov't

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