A new genetic locus for X linked progressive cone-rod dystrophy

X linked progressive cone-rod dystrophy (COD) is a retinal disease primarily affecting the cone photoreceptors. The disease is genetically heterogeneous and two loci, COD1 (Xp21.1-11.4) and COD2 (Xq27.2-28), have been previously identified. COD1 was recently shown to be caused by mutations in RPGR e...

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Autors principals: Jalkanen, R, Demirci, F, Tyynismaa, H, Bech-Hansen, T, Meindl, A, Peippo, M, Mantyjarvi, M, Gorin, M, Alitalo, T
Format: Artigo
Idioma:Inglês
Publicat: BMJ Group 2003
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Original Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC1735490/
https://ncbi.nlm.nih.gov/pubmed/12807962
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.40.6.418
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