A detailed study of the phenotype of an autosomal dominant cone-rod dystrophy (CORD7) associated with mutation in the gene for RIM1

M. Michaelides, G.E. Holder, David Hunt, F.W. Fitzke, A.C. Bird, A.T. Moore

Research output: Contribution to journal › Article › peer-review

Original language	English
Pages (from-to)	198-206
Journal	British Journal of Opthalmology
Volume	89
DOIs	https://doi.org/10.1136/bjo.2004.050773
Publication status	Published - 2005

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title = "A detailed study of the phenotype of an autosomal dominant cone-rod dystrophy (CORD7) associated with mutation in the gene for RIM1",

author = "M. Michaelides and G.E. Holder and David Hunt and F.W. Fitzke and A.C. Bird and A.T. Moore",

year = "2005",

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journal = "British Journal of Opthalmology",

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T1 - A detailed study of the phenotype of an autosomal dominant cone-rod dystrophy (CORD7) associated with mutation in the gene for RIM1

AU - Michaelides, M.

AU - Holder, G.E.

AU - Hunt, David

AU - Fitzke, F.W.

AU - Bird, A.C.

AU - Moore, A.T.

PY - 2005

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U2 - 10.1136/bjo.2004.050773

DO - 10.1136/bjo.2004.050773

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SN - 0007-1161

VL - 89

SP - 198

EP - 206

JO - British Journal of Opthalmology

JF - British Journal of Opthalmology

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