A novel MERTK mutation causing retinitis pigmentosa-Reference-Cited by-同舟云学术

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A novel MERTK mutation causing retinitis pigmentosa

Published:2017-05-01 Issue:8 Volume:255 Page:1613-1619
ISSN:0721-832X
Container-title:Graefe's Archive for Clinical and Experimental Ophthalmology
language:en
Short-container-title:Graefes Arch Clin Exp Ophthalmol

Author:

Al-khersan Hasenin,Shah Kaanan P.,Jung Segun C.,Rodriguez Alex,Madduri Ravi K.,Grassi Michael A.

Funder

National Eye Institute

Search for Vision

Research to Prevent Blindness

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Sensory Systems,Ophthalmology

Link

http://link.springer.com/article/10.1007/s00417-017-3679-9/fulltext.html

Reference29 articles.

1. Evans RJ, Schwarz N, Nagel-Wolfrum K, Wolfrum U, Hardcastle AJ, Cheetham ME (2010) The retinitis pigmentosa protein RP2 links pericentriolar vesicle transport between the Golgi and the primary cilium. Hum Mol Gen 19:1358–1367. doi: 10.1093/hmg/ddq012

2. Busskamp V, Duebel J, Balya D et al (2010) Genetic reactivation of cone photoreceptors restores visual responses in retinitis pigmentosa. Science 329:413–417. doi: 10.1126/science.1190897

3. Hartong DT, Berson EL, Dryja TP (2006) Retinitis pigmentosa. Lancet 368:1795–1809. doi: 10.1016/S0140-6736(06)69740-7

4. Farrar G, Kenna PF, Humphries P (2002) New EMBO member’s review: on the genetics of retinitis pigmentosa and on mutation-independent approaches to therapeutic intervention. EMBO J 21:857–864. doi: 10.1093/emboj/21.5.857

5. Ferrari S, Di Iorio E, Barbaro V, Ponzin D, Sorrentino FS, Parmeggiani F (2011) Retinitis pigmentosa: genes and disease mechanisms. Curr Genomics 12:238–249. doi: 10.2174/138920211795860107

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