A mutation in NRL is associated with autosomal dominant retinitis pigmentosa

Citation
Dar. Bessant et al., A mutation in NRL is associated with autosomal dominant retinitis pigmentosa, NAT GENET, 21(4), 1999, pp. 355-356
Citations number
15
Categorie Soggetti
Molecular Biology & Genetics
Journal title
NATURE GENETICS
ISSN journal
10614036 → ACNP
Volume
21
Issue
4
Year of publication
1999
Pages
355 - 356
Database
ISI
SICI code
1061-4036(199904)21:4<355:AMINIA>2.0.ZU;2-3