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Tobias Schulte-Middelmann

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Human Molecular Genetics|June 18, 2011

Ccdc66 null mutation causes retinal degeneration and dysfunctionWanda M Gerding, Sabrina Schreiber, Tobias Schulte-Middelmann, et al.

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Human Molecular Genetics|June 18, 2011

Ccdc66 null mutation causes retinal degeneration and dysfunctionWanda M Gerding, Sabrina Schreiber, Tobias Schulte-Middelmann, et al.

Pageof 1