A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Starqardt macular dystrophy

Author:

Allikmets Rando,Singh Nanda,Sun Hui,Shroyer Noah F.,Hutchinson Amy,Chidambaram Abirami,Gerrard Bernard,Baird Lisa,Stauffer Dora,Peiffer Andy,Rattner Amir,Smallwood Philip,Li Yixin,Anderson Kent L.,Lewis Richard Alan,Nathans Jeremy,Leppert Mark,Dean Michael,Lupski James R.

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Reference77 articles.

1. National Advisory Eye Council. Vision Research, a National Plan, 1994-1998. National Institutes of Health publication 93–3186 (1993).

2. Blacharski, P.A. Fundus flavimaculatus. in Retinal dystrophies and degenerations,(ed. Newsome, D.A.) 135–159 (New York: Raven Press, 1988).

3. Stargardt, K. U¨ber fämiliare, progressive degeneration in der maculagegend des auges. Albrechtvon Graefes. Arch Klin. Exp. Ophthalmol. 71, 534–550 (1909).

4. Anderson, K.L. et al. A YAC contig encompassing the recessive Stargardt disease gene (STGD) on chromosome 1p. Am. J. Hum. Genet. 57, 1351–1363 (1995).

5. Franceschetti, A. Über tapeto-retinale degenerationen im kindesalter. in Entwicklung und fortschritt in der augenheilkunde. (ed von Sautter, H.) 107–120 (Stuttgart: Ferdinand Enke, 1963).

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