Heterozygous missense mutation in the rhodopsin gene as a cause of congenital stationary night blindness-Reference-Cited by-同舟云学术

Heterozygous missense mutation in the rhodopsin gene as a cause of congenital stationary night blindness

Published:1993-07 Issue:3 Volume:4 Page:280-283
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Dryja Thaddeus P.,Berson Eliot L.,Rao Vikram R.,Oprian Daniel D.

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng0793-280.pdf

Reference29 articles.

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2. Goodman, G. & Bornschein, H. Comparative electroretinographic studies in congenital night blindness and total color blindness. Arch. Ophthalmol. 58, 174–182 (1957).

3. Hill, D.A., Arbel, K.F. & Berson, E.L. Cone electroretinograms in congenital nyctalopia with myopia. Am. J. Ophthalmol. 78, 127–136 (1974).

4. Carr, R.E., Ripps, H., Siegel, I.M. & Weale, R.A. Rhodopsin and the electrical activity of the retina in congenital night blindness. Invest. Ophthal. Vis. Sci. 5, 497–507 (1966).

5. Peachey, N.S. et al. A form of congenital stationary night blindness with apparent defect of rod phototransduction. Invest. Ophthal. Vis. Sci. 31, 237–246 (1990).

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