Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleExome sequencing identifies PEX6 mutations in three cases diagnosed with Retinitis Pigmentosa and hearing impairment.AuthorsGarcía-García, Gema; Sanchez-Navarro, Iker; Aller, Elena; Jaijo, Teresa; Fuster-Garcia, Carla; Rodríguez-Munoz, Ana; Vallejo, Elena; José Tellería, Juan; Vázquez, Selma; Beltrán, Sergi; Derdak, Sophia; Zurita, Olga; Villaverde-Montero, Cristina; Avila-Fernández, Almudena; Corton, Marta; Blanco-Kelly, Fiona; Hakonarson, Hakon; Millán, José M.; Ayuso, CarmenPublicationMolecular Vision, 2020, Vol 26, p216ISSN1090-0535Publication typeArticle