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August 1, 1999Human Molecular Genetics

RPGR Transcription Studies in Mouse and Human Tissues Reveal a Retina-Specific Isoform That Is Disrupted in a Patient With X-Linked Retinitis Pigmentosa

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Authors

RKRenate Kirschner‐SchwabeKrankenhaus St. Joseph-Stift BremenTRThomas RosenbergCopenhagen University HospitalRSRobert Schultz‐HeienbrokBerlin Heart (Germany)

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Cite This Study

Kirschner‐Schwabe et al. (1999) studied this question.

synapsesocial.com/papers/6a7af4841a7b6c10bc0db603https://doi.org/10.1093/hmg/8.8.1571
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Also Consider

Synapse has enriched 4 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Solubilization of Membrane-bound Rod Phosphodiesterase by the Rod Phosphodiesterase Recombinant δ Subunit1996 · 91 citations
  2. 2The retinitis pigmentosa GTPase regulator, RPGR, interacts with the delta subunit of rod cyclic GMP phosphodiesterase1999 · 124 citations
  3. 3Biochemical Characterization and Subcellular Localization of the Mouse Retinitis Pigmentosa GTPase Regulator (mRpgr)1998 · 79 citations
  4. 4Genomic Structure and Comparative Analysis of Nine <i>Fugu</i> Genes: Conservation of Synteny with Human Chromosome Xp22.2–p22.11999 · 44 citations