Next generation sequencing-based molecular diagnosis of retinitis pigmentosa: identification of a novel genotype-phenotype correlation and clinical refinementsFeng Wang, Rui Chen, Irma López et al.|Human Genetics|2013Cited by 242
Progressive photoreceptor degeneration, outer segment dysplasia, and rhodopsin mislocalization in mice with targeted disruption of the retinitis pigmentosa-1 ( <i>Rp1</i> ) geneJiangang Gao, Jianping Zuo, Kyeongmi Cheon et al.|Proceedings of the National Academy of Sciences|2002Cited by 134
Identification and subcellular localization of the RP1 protein in human and mouse photoreceptors.Qin Liu, Eric A. Pierce, Jie Zhou et al.|PubMed|2002Cited by 134
Identification of Disease-Causing Mutations in Autosomal Dominant Retinitis Pigmentosa (adRP) Using Next-Generation DNA SequencingSara J. Bowne, Stephen P. Daiger, Lori S. Sullivan et al.|Investigative Ophthalmology & Visual Science|2010Cited by 79
Why Do Mutations in the Ubiquitously Expressed Housekeeping Gene<i>IMPDH1</i>Cause Retina-Specific Photoreceptor Degeneration?Sara J. Bowne, Stephen P. Daiger, Qin Liu et al.|Investigative Ophthalmology & Visual Science|2006Cited by 71