Mutations in MERTK, the human orthologue of the RCS rat retinal dystrophy gene, cause retinitis pigmentosa
Gal, Andreas, Li, Yun, Thompson, Debra A., Weir, Jessica, Orth, Ulrike, Jacobson, Samuel G., Apfelstedt-Sylla, Eckart, Vollrath, Douglas·2000·Nature Genetics
DOI 10.1038/81555
Cited by (680)
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