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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Mutations in the RPGR gene cause X-linked cone dystrophy

By Yang Z.  

Human Molecular Genetics, Vol. 11, Iss. 5, 2002-03 ,pp. : 605-611

Oxford University Press

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New mutations in MID1 provide support for loss of function as the cause of X-linked Opitz syndrome

By Cox Timothy C.  

Human Molecular Genetics, Vol. 9, Iss. 17, 2000-10 ,pp. : 2553-2562

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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Localization in the human retina of the X-linked retinitis pigmentosa protein RP2, its homologue cofactor C and the RP2 interacting protein Arl3

By Cheetham M.E.  

Human Molecular Genetics, Vol. 11, Iss. 24, 2002-09 ,pp. : 3065-3074

Oxford University Press

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