Electroretinographic anomalies in mice with mutations in Myo7a, the gene involved in human Usher syndrome type 1B. [electronic resource]

By: Contributor(s): Producer: 20010315Description: 770-8 p. digitalISSN:
  • 0146-0404
Subject(s): In: Investigative ophthalmology & visual science vol. 42
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't

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