Zrenner, Eberhart

Mutations in RPE65 cause Leber's congenital amaurosis

Marlhens, F., Bareil, C., Griffoin, J.-M., Zrenner, E., Amalric, P., Eliaou, C., Liu, S.-Y., Harris, E., Redmond, T. M., Arnaud, B., et al. (1997) · Nature Genetics

Retinal Development and DisordersRetinal Diseases and Treatments

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Epidemiology of Major Eye Diseases Leading to Blindness in Europe: A Literature Review

Prokofyeva, E., & Zrenner, E. (2012) · Ophthalmic Research

Ophthalmology and Visual Impairment StudiesRetinal Diseases and Treatments

Cited by 212

Biochemical but not clinical vitamin A deficiency results from mutations in the gene for retinol binding protein

Biesalski, H. K., Frank, J., Beck, S. C., Heinrich, F., Illek, B., Reifen, R., Gollnick, H., Seeliger, M. W., Wissinger, B., & Zrenner, E. (1999) · The American Journal of Clinical Nutrition

Retinal Development and DisordersRetinoids in leukemia and cellular processes

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