Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
9346084 | Ophthalmology | 2005 | 9 Pages |
Abstract
The X-linked cone dysfunction syndrome associated with myopia and dichromacy described here has many similarities to Bornholm eye disease, a condition previously mapped to Xq28. Except for the Cys203Arg substitution in one family, no alterations in the opsin gene array were identified that could underlie the cone dysfunction. It is therefore possible that the cone dysfunction may have a genetic origin different from that of the dichromacy.
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Authors
Michel BSc, MRCOphth, Samantha BSc, PhD, Keith BSc, PhD, Graham E. BSc, PhD, Matthew P. BSc, PhD, John D. (FRS), Anthony T. (FRCOphth), David M. BSc, PhD,