Autosomal recessive retinitis pigmentosa and cone-rod dystrophy caused by splice site mutations in the Stargardt's disease gene ABCR
Number of pages
SourceHuman Molecular Genetics, 7, (1998), pp. 355-362
Article / Letter to editor
Display more detailsDisplay less details
Human Molecular Genetics
Upload full text
Use your RU credentials (u/z-number and password) to log in with SURFconext to upload a file for processing by the repository team.