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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

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Bernhard H. F. Weber

Institut für Humangenetik der Universität

Biozentrum

Würzburg

Deutschland

[email]@*.uni-wuerzburg.de

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Affiliations

Institut für Humangenetik der Universität, Biozentrum, Würzburg, Deutschland. 1998 - 2002
Institute of Human Genetics, Biocenter, University of Würzburg, D-97074 Würzburg, Germany. 2002

References

Inactivation of the murine X-linked juvenile retinoschisis gene, Rs1h, suggests a role of retinoschisin in retinal cell layer organization and synaptic structure. Weber, B.H., Schrewe, H., Molday, L.L., Gehrig, A., White, K.L., Seeliger, M.W., Jaissle, G.B., Friedburg, C., Tamm, E., Molday, R.S. Proc. Natl. Acad. Sci. U.S.A. (2002) [Pubmed]
A mouse model for Sorsby fundus dystrophy. Weber, B.H., Lin, B., White, K., Kohler, K., Soboleva, G., Herterich, S., Seeliger, M.W., Jaissle, G.B., Grimm, C., Reme, C., Wenzel, A., Asan, E., Schrewe, H. Invest. Ophthalmol. Vis. Sci. (2002) [Pubmed]
Recent advances in the molecular genetics of hereditary retinal dystrophies with primary involvement of the macula. Weber, B.H. Acta. Anat. (Basel) (1998) [Pubmed]