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RPGR mutation associated with retinitis pigmentosa, impaired hearing, and sinorespiratory infections

Zito, I; Downes, SM; Patel, RJ; Cheetham, ME; Ebenezer, ND; Jenkins, SA; Bhattacharya, SS; ... Hardcastle, AJ; + view all (2003) RPGR mutation associated with retinitis pigmentosa, impaired hearing, and sinorespiratory infections. J MED GENET , 40 (8) 609 - 615. Green open access

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Type: Article
Title: RPGR mutation associated with retinitis pigmentosa, impaired hearing, and sinorespiratory infections
Open access status: An open access version is available from UCL Discovery
Keywords: PRIMARY CILIARY DYSKINESIA, LEBER CONGENITAL AMAUROSIS, NUCLEOTIDE-EXCHANGE FACTOR, USHER-SYNDROME, IMMOTILE-CILIA, NASAL CILIA, CYTOPLASMIC DYNEIN, POSITIONAL CLONING, LIGHT-CHAINS, EXON ORF15
UCL classification: UCL
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > Institute of Ophthalmology
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > The Ear Institute
URI: https://discovery.ucl.ac.uk/id/eprint/7292
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