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X-linked cone-rod dystrophy

Brown J, Jr., Kimura AE, Gorin MB (2000) Clinical and electroretinographic findings of female carriers and affected males in a progressive X-linked cone-rod dystrophy (COD-1) pedigree. Ophthalmology 107 1104-1110. [Pg.244]

Jalkanen R, Mantyjarvi M, Tobias R, Isosomppi J, Sankila EM, Alitalo T, Bech-Hansen NT (2006) X-linked cone-rod dystrophy, CORDX3, is caused by a mutation in the CACNA1F gene. J Med Genet. [Pg.246]


See other pages where X-linked cone-rod dystrophy is mentioned: [Pg.215]    [Pg.228]    [Pg.230]    [Pg.215]    [Pg.228]    [Pg.230]    [Pg.1332]    [Pg.419]    [Pg.398]   
See also in sourсe #XX -- [ Pg.215 , Pg.228 , Pg.230 , Pg.231 ]




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