Mutations in MERTK, the human orthologue of the RCS rat retinal dystrophy gene, cause retinitis pigmentosa
Andreas Gal(Eppendorf (Germany)), Yun Li(Eppendorf (Germany)), Debra A. Thompson(University of Michigan–Ann Arbor), Jessica Weir(Stanford University), Ulrike Orth(Eppendorf (Germany)), Samuel G. Jacobson(Penn Presbyterian Medical Center), Eckart Apfelstedt-Sylla(STZ eyetrial), Douglas Vollrath(Stanford University)
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