Mutations in a gene encoding a new oxygen-regulated photoreceptor protein cause dominant retinitis pigmentosa-Reference-Cited by-同舟云学术

Mutations in a gene encoding a new oxygen-regulated photoreceptor protein cause dominant retinitis pigmentosa

Published:1999-07 Issue:3 Volume:22 Page:248-254
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Pierce Eric A.,Quinn Tracey,Meehan Terrence,McGee Terri L.,Berson Eliot L.,Dryja Thaddeus P.

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng0799_248.pdf

Reference35 articles.

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2. Dryja, T.P. Genetic heterogeneity of retinal degenerations and dysfunctions. Les Seminaires Ophtalmologiques d'ISPEN 10, 25– 35 (1998).

3. Dryja, T.P. & Li, T. Molecular genetics of retinitis pigmentosa. Hum. Mol. Genet. 4, 1739– 1743 (1995).

4. Berson, E.L. Retinitis pigmentosa: unfolding its mystery. Proc. Natl Acad. Sci. USA 93, 4526–4528 ( 1996).

5. Spence, M.A. et al. Probable genetic linkage between autosomal dominant retinitis pigmentosa (RP) and amylase (AMY 2): evidence of an RP locus on chromosome 1. Am. J. Hum. Genet. 29, 397–404 (1977); erratum: 29, 592 (1977).

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