Drupal-Biblio17<style face="normal" font="default" size="100%">The mechanistic functional landscape of retinitis pigmentosa: a machine learning-driven approach to therapeutic target discovery.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Primary Ciliary Dyskinesia and Retinitis Pigmentosa: Novel Variant and Possible Modifier Gene.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Identification of the Photoreceptor Transcriptional Co-Repressor SAMD11 as Novel Cause of Autosomal Recessive Retinitis Pigmentosa.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Re-evaluation casts doubt on the pathogenicity of homozygous USH2A p.C759F.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Whole-exome sequencing reveals ZNF408 as a new gene associated with autosomal recessive retinitis pigmentosa with vitreal alterations.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Novel RP1 mutations and a recurrent BBS1 variant explain the co-existence of two distinct retinal phenotypes in the same pedigree.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Mutation screening of multiple genes in Spanish patients with autosomal recessive retinitis pigmentosa by targeted resequencing.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Mutation spectrum of EYS in Spanish patients with autosomal recessive retinitis pigmentosa.</style>