NR2E3 mutations in enhanced S-cone sensitivity syndrome (ESCS), Goldmann-Favre syndrome (GFS), clumped pigmentary retinal degeneration (CPRD), and retinitis pigmentosa (RP). [electronic resource]

By: Contributor(s): Producer: 20100225Description: 1475-85 p. digitalISSN:
  • 1098-1004
Subject(s): Online resources: In: Human mutation vol. 30
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Review

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