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Items: 4

1.

Deletion of the X-linked opsin gene array locus control region (LCR) results in disruption of the cone mosaic.

Carroll J, Rossi EA, Porter J, Neitz J, Roorda A, Williams DR, Neitz M.

Vision Res. 2010 Sep 15;50(19):1989-99. doi: 10.1016/j.visres.2010.07.009. Epub 2010 Jul 16.

2.

Molecular genetics of color-vision deficiencies.

Deeb SS.

Vis Neurosci. 2004 May-Jun;21(3):191-6. Review.

PMID:
15518188
3.

[Inherited colour vision deficiencies--from Dalton to molecular genetics].

Cvetković D, Cvetković D.

Srp Arh Celok Lek. 2005 Nov-Dec;133(11-12):521-7. Review. Serbian.

4.

The cone dysfunction syndromes.

Aboshiha J, Dubis AM, Carroll J, Hardcastle AJ, Michaelides M.

Br J Ophthalmol. 2016 Jan;100(1):115-21. doi: 10.1136/bjophthalmol-2014-306505. Epub 2015 Mar 13. Review.

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