Mutations in MERTK, the human orthologue of the RCS rat retinal dystrophy gene, cause retinitis pigmentosa.
Gal A; Li Y; Thompson DA; Weir J; Orth U; Jacobson SG; Apfelstedt-Sylla E; Vollrath D; Nature Genetics, 2000, vol. 26, issue 3, p 270, ISSN 10614036. ISBN 10614036.

Full Text Resources Located for this Citation

View article on EBSCOhost(Login required)
View article via Electronic Journal Services