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

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite

Deep intronic mutation in OFD1 , identified by targeted genomic next-generation sequencing, causes a severe form of X-linked retinitis pigmentosa (RP23)

By Webb Tom R.   Parfitt David A.   Gardner Jessica C.   Martinez Ariadna   Bevilacqua Dalila   Davidson Alice E.   Zito Ilaria   Thiselton Dawn L.   Ressa Jacob H.C.   Apergi Marina   Schwarz Nele   Kanuga Naheed   Michaelides Michel   Cheetham Michael E.   Gorin Michael B.   Hardcastle Alison J.  

Human Molecular Genetics, Vol. 21, Iss. 16, 2012-08 ,pp. : 3647-3654

Oxford University Press

Access to resources Recommend Favorite