RPGR transcription studies in mouse and human tissues reveal a retina-specific isoform that is disrupted in a patient with X-linked retinitis pigmentosa

By Kirschner Renate  

Human Molecular Genetics, Vol. 8, Iss. 8, 1999-08 ,pp. : 1571-1578

Oxford University Press

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Positional Cloning of the Gene for X-Linked Retinitis Pigmentosa 3: Homology with the Guanine-Nucleotide-Exchange Factor RCC1

By Roepman Ronald  

Human Molecular Genetics, Vol. 5, Iss. 7, 1996-01 ,pp. : 1035-1041

Oxford University Press

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Mapping of X-linked progressive retinal atrophy (XLPRA), the canine homolog of retinitis pigmentosa 3 (RP3)

By Zeiss Caroline J.   Ray Kunal   Acland Gregory M.   Aguirre Gustavo D.  

Human Molecular Genetics, Vol. 9, Iss. 4, 2000-03 ,pp. : 531-537

Oxford University Press

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Mutations in the N-terminus of the X-linked retinitis pigmentosa protein RP2 interfere with the normal targeting of the protein to the plasma membrane

By Chapple J. Paul   Hardcastle AlisonJ.  

Human Molecular Genetics, Vol. 9, Iss. 13, 2000-08 ,pp. : 1919-1926

Oxford University Press

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The X-linked retinitis pigmentosa protein RP2 facilitates G protein traffic

By Schwarz Nele   Novoselova Tatiana V.   Wait Robin   Hardcastle Alison J.   Cheetham Michael E.  

Human Molecular Genetics, Vol. 21, Iss. 4, 2012-02 ,pp. : 863-873

Oxford University Press

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