Orth, Ulrike

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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Missense rhodopsin mutation in a family with recessive RP

Kumaramanickavel, G., Maw, M., Denton, M. J., John, S., Srikumari, C. R. S., Orth, U., Oehlmann, R., & Gal, A. (1994) · Nature Genetics

Retinal Development and DisordersGenetic and Kidney Cyst Diseases

Cited by 94