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July 10, 2003Clinical Genetics

Analysis of RPGR in a South African family with X‐linked retinitis pigmentosa: research and diagnostic implications

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Authors

GRGeorge RebelloUniversity of Cape TownAVAlvera VorsterStellenbosch UniversityJGJacquie GreenbergUniversity of Cape Town

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Rebello et al. (2003) studied this question.

synapsesocial.com/papers/6a22c0981ee3c9daa9cd7a96https://doi.org/10.1034/j.1399-0004.2003.00090.x
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Also Consider

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

  1. 1The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools1997 · 39,299 citations
  2. 2RPGR Transcription Studies in Mouse and Human Tissues Reveal a Retina-Specific Isoform That Is Disrupted in a Patient With X-Linked Retinitis Pigmentosa1999 · 147 citations
  3. 3Localizing multiple X chromosome-linked retinitis pigmentosa loci using multilocus homogeneity tests.1990 · 228 citations
  4. 4Spectrum of Mutations in the RPGR Gene That Are Identified in 20% of Families with X-Linked Retinitis Pigmentosa1997 · 99 citations