Ryan Crane
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Publications 4
- The usherin mutation c.2299delG leads to its mislocalization and disrupts interactions with whirlin and VLGR1.
- Comparative study of PRPH2 D2 loop mutants reveals divergent disease mechanism in rods and cones.
- Correction: Comparative study of PRPH2 D2 loop mutants reveals divergent disease mechanism in rods and cones.
- Riboflavin deficiency leads to irreversible cellular changes in the RPE and disrupts retinal function through alterations in cellular metabolic homeostasis.
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