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October 1, 1991Proceedings of the National Academy of SciencesOpen Access

Functional heterogeneity of mutant rhodopsins responsible for autosomal dominant retinitis pigmentosa.

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Authors

CSChing‐Hwa SungCornell UniversityBSBarbara SchneiderAltonaer KinderkrankenhausNANeeraj AgarwalHuntsman Cancer Institute

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Cite This Study

Sung et al. (1991) studied this question.

synapsesocial.com/papers/6a7cd82762c4fb5458aeb096https://doi.org/10.1073/pnas.88.19.8840
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Role of the intradiscal domain in rhodopsin assembly and function.1990 · 140 citations
  2. 2Rapid embedding of tissues in Lowicryl K4M for immunoelectron microscopy.1984 · 266 citations
  3. 3In vitro biosynthesis, core glycosylation and membrane integration of opsin1981 · 49 citations
  4. 4THE LDL RECEPTOR LOCUS IN FAMILIAL HYPERCHOLESTEROLEMIA: Mutational Analysis of a Membrane Protein1990 · 700 citations
  5. 5Mutations within the Rhodopsin Gene in Patients with Autosomal Dominant Retinitis Pigmentosa1990 · 509 citations