| 1 | CACNA1F, CORDX3
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| A novel large in-frame deletion within the CACNA1F gene associates with a cone-rod dystrophy 3-like phenotype.
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| Hauke J, Schild A, Neugebauer A, Lappa A, Fricke J, Fauser S, Rösler S, Pannes A, Zarrinnam D, Altmüller J, Motameny S, Nürnberg G, Nürnberg P, Hahnen E, Beck BB.
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| PLoS One 8(10):e76414. doi: 10.1371/journal.pone.0076414. eCollection 2013.
2013
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| 2 | CORDX3, CACNA1F
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| X linked cone-rod dystrophy, CORDX3, is caused by a mutation in the CACNA1F gene.
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| Jalkanen R, Mantyjarvi M, Tobias R, Isosomppi J, Sankila EM, Alitalo T, Bech-Hansen NT.
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| J Med Genet 43(8):699-704. Epub 2006 Feb 27. 2006
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| 3 | CORDX3, CORDX1
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| A new genetic locus for X linked progressive cone-rod dystrophy.
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| Jalkanen R, Demirci FY, Tyynismaa H, Bech-Hansen T, Meindl A, Peippo M, Mantyjarvi M, Gorin MB, Alitalo T.
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| J Med Genet 40(6):418-23. 2003
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| 4 | CORDX3
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| X linked progressive cone dystrophy. Localisation of the gene locus to Xp21-p11.1 by linkage analysis.
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| Meire FM, Bergen AA, De Rouck A, Leys M, Delleman JW.
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| Br J Ophthalmol 78(2):103-8. 1994
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