Molekulare Grundlagen erblicher Netzhautdegenerationen: Retinitis pigmentosa, Zapfen- und Makuladystrophien

Author:

Apfelstedt-Sylla Eckart,Gal Andreas,Weber Bernhard H. F.

Publisher

Springer Berlin Heidelberg

Reference182 articles.

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2. Al-Maghtheh M., Vithana E., Tarttelin E. et al. (1996) Evidence for a major retinitis pigmentosa locus on 19q13.4 (RP11), and association with a unique bimodal expressivity phenotype. Am J Hum Genet 59:864–871

3. Allikmets R., Shroyer N.F., Singh N. et al. (1997a) Mutation of the Stargardt disease gene (ABCR) in age-related macular degeneration. Science 277:1805–1807

4. Allikmets R., Singh N., Sun H. et al. (1997b) A photoreceptor cell specific ATP binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy. Nat Genet 15:236–246

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