Apfelstedt-Sylla, Eckart

Mutations in MERTK, the human orthologue of the RCS rat retinal dystrophy gene, cause retinitis pigmentosa

Gal, A., Li, Y., Thompson, D. A., Weir, J., Orth, U., Jacobson, S. G., Apfelstedt-Sylla, E., & Vollrath, D. (2000) · Nature Genetics

Retinal Development and DisordersRetinal Diseases and Treatments

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Mutations in the gene encoding lecithin retinol acyltransferase are associated with early-onset severe retinal dystrophy

Thompson, D. A., Li, Y., McHenry, C. L., Carlson, T. J., Ding, X., Sieving, P. A., Apfelstedt-Sylla, E., & Gal, A. (2001) · Nature Genetics

Retinal Development and DisordersRetinoids in leukemia and cellular processes

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