DOI:
10.1055/s-00000031
Klinische Monatsblätter für Augenheilkunde
LinksClose Window
References
Gal A, Li Y, Thompson DA. et al.
Mutations in MERTK, the human orthologue of the RCS rat retinal dystrophy gene, cause retinitis pigmentosa.
Nat Genet 2000;
26: 270-271
We do not assume any responsibility for the contents of the web pages of other providers.