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Keywords: RP2
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Journal Articles
J Cell Sci (2018) 131 (4): jcs211748.
Published: 20 February 2018
...Rodanthi Lyraki; Mandy Lokaj; Dinesh C. Soares; Abigail Little; Matthieu Vermeren; Joseph A. Marsh; Alfred Wittinghofer; Toby Hurd ABSTRACT Retinitis pigmentosa 2 ( RP2 ) is the causative gene for a form of X-linked retinal degeneration. RP2 was previously shown to have GTPase-activating protein...
Includes: Supplementary data
Journal Articles
J Cell Sci (2011) 124 (5): 718–726.
Published: 1 March 2011
...Toby W. Hurd; Shuling Fan; Ben L. Margolis Ciliopathies represent a newly emerging group of human diseases that share a common etiology resulting from dysfunction of the cilium or centrosome. The gene encoding the retinitis pigmentosa 2 protein (RP2) is mutated in X-linked retinitis pigmentosa. RP2...
Includes: Supplementary data