A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X–linked retinitis pigmentosa (RP3)
Meindl, A. ; Dry, K. ; Herrmann, K. ; Manson, E. ; Ciccodicola, A. ; Edgar, A. ; Carvalho, M.R.S. ; Achatz, H. ; Hellebrand, H. ; Lennon, A. ; Migliaccio, C. ; Porter, K. ; Zrenner, E. ; Bird, A. ; Jay, M. ; Lorenz, B. ; Wittwer, B. ; D'Urso, M. ; Meitinger, T. ; Wright, A.
[s.l.] : Nature Publishing Group
Published 1996
[s.l.] : Nature Publishing Group
Published 1996
| ISSN: |
1546-1718
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| Source: |
Nature Archives 1869 - 2009
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| Topics: |
Biology
Medicine
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| Notes: |
[Auszug] X-linked retinitis pigmentosa (xIRP) is a severe progressive retinal degeneration which affects about 1 in 25,000 of the population. The most common form of xIRR RP3, has been localised to the interval between CYBB and OTC in Xp21.1 by linkage analysis and deletion mapping. Identification of ...
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| Type of Medium: |
Electronic Resource
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| URL: |