A hypothesis to explain the reduced blood levels of docosahexaenoic acid in inherited retinal degenerations caused by mutations in genes encoding retina-specific proteins

Author:

Anderson Robert E.,Maude Maureen B.,Alvarez Richard A.,Acland Gregory,Aguirre Gustavo D.

Publisher

Wiley

Subject

Cell Biology,Organic Chemistry,Biochemistry

Reference25 articles.

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2. Converse, C., McLachlan, T., Bow, A., Packard, C., and Shepherd, J. (1987). Lipid Metabolism in Retinitis Pigmentosa, inDegenerative Retinal Disorders, Clinical and Laboratory Investigations (Hollyfield, J., Anderson, R., and LaVail, M., eds.) pp. 93–101, Alan R. Liss Inc., New York.

3. Anderson, R., Maude, M., Lewis, R., Newsome, D., and Fishman, G. (1987) Abnormal Plasma Levels of Polyunsaturated Fatty Acid in Autosomal Dominant Retinitis Pigmentosa,Exp. Eye Res. 44, 155–159.

4. Gong, J., Rosner, B., Rees, D., Berson, E., Weigel-DiFranco, C., and Schaefer, E. (1992) Plasma Docosahexaenoic Acid Levels in Various Genetic Forms of Retinitis Pigmentosa,Invest. Ophthalmol. Vis. Sci. 33, 2596–2602.

5. Hoffman, D., Uauy, R., and Birch, D. (1993) Red Blood Cell Fatty Acid Levels in Patients with Autosomal Dominant Retinitis Pigmentosa,Exp. Eye. Res. 57, 359–368.

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