Usher syndrome and Leber congenital amaurosis are molecularly linked via a 
novel isoform of the centrosomal ninein-like protein

van Wijk, E.; Kersten, F. F. J.; Kartono, A.; Mans, D. A.; Brandwijk, K.; Letteboer, S. J. F.; Peters, T. A.; Marker, T.; Yan, X. M.; Cremers, C. W. R. J.; Cremers, F. P. M.; Wolfrum, U.; Roepman, R.; Kremer, H.

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Usher syndrome and Leber congenital amaurosis are molecularly linked via a novel isoform of the centrosomal ninein-like protein

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Yan, X. M.
Former Research Groups, Max Planck Institute of Biochemistry, Max Planck Society;

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van Wijk, E., Kersten, F. F. J., Kartono, A., Mans, D. A., Brandwijk, K., Letteboer, S. J. F., et al. (2009). Usher syndrome and Leber congenital amaurosis are molecularly linked via a novel isoform of the centrosomal ninein-like protein. Human Molecular Genetics, 18(1), 51-64.

Cite as: https://hdl.handle.net/11858/00-001M-0000-0010-5AB1-A

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