A mutation in NRL is associated with autosomal dominant retinitis pigmentosa.
Bessant DA; Payne AM; Mitton KP; Wang QL; Swain PK; Plant C; Bird AC; Zack DJ; Swaroop A; Bhattacharya SS; Nature Genetics, 1999, vol. 21, issue 4, p 355, ISSN 10614036. ISBN 10614036.

Full Text Resources Located for this Citation

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