Novel compound heterozygous mutation in the POC1B gene underlie peripheral cone dystrophy in a Chinese family. [electronic resource]

By: Contributor(s): Producer: 20190410Description: 300-306 p. digitalISSN:
  • 1744-5094
Subject(s): Online resources: In: Ophthalmic genetics vol. 39
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

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