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  • D. T. Hartong, E. Berson, T. Dryja
  • Medicine
  • The Lancet
  • 2006 (First Publication: 24 November 2006)
  • Hereditary degenerations of the human retina are genetically heterogeneous, with well over 100 genes implicated so far. This Seminar focuses on the subset of diseases called retinitis pigmentosa, inExpand
  • D. Hong, B. Pawlyk, J. Shang, M. Sandberg, E. Berson, T. Li
  • Biology, Medicine
  • Proceedings of the National Academy of Sciences…
  • 2000 (First Publication: 28 March 2000)
  • The X-linked RP3 locus codes for retinitis pigmentosa GTPase regulator (RPGR), a protein of unknown function with sequence homology to the guanine nucleotide exchange factor for Ran GTPase. WeExpand
  • D. Sharon, M. Sandberg, Vivian W. Rabe, Melissa A. Stillberger, T. Dryja, E. Berson
  • Medicine, Biology
  • American journal of human genetics
  • 2003 (First Publication: 1 November 2003)
  • We determined the mutation spectrum of the RP2 and RPGR genes in patients with X-linked retinitis pigmentosa (XLRP) and searched for correlations between categories of mutation and severity ofExpand
  • Eric A. Pierce, Tracey Quinn, Terrence F Meehan, T. L. McGee, Eliot L. Berson, T. P. Dryja
  • Biology, Medicine
  • Nature Genetics
  • 1999 (First Publication: 1 July 1999)
  • The autosomal dominant retinitis pigmentosa (RP) locus, designated RP1, has been mapped through linkage studies to a 4-cM interval at 8q11–13. Here we describe a new photoreceptor-specific gene thatExpand
  • T. Dryja, T. McGee, +5 authors Aruna S. Rajagopalan
  • Medicine, Biology
  • Proceedings of the National Academy of Sciences…
  • 2005 (First Publication: 29 March 2005)
  • We report three unrelated patients with mutations in the GRM6 gene that normally encodes the glutamate receptor mGluR6. This neurotransmitter receptor has been shown previously to be present only inExpand