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Mutations in ARL2BP, Encoding ADP-Ribosylation-Factor-Like 2 Binding Protein, Cause Autosomal-Recessive Retinitis Pigmentosa

Davidson, AE; Schwarz, N; Zelinger, L; Stern-Schneider, G; Shoemark, A; Spitzbarth, B; Gross, M; ... Webster, AR; + view all (2013) Mutations in ARL2BP, Encoding ADP-Ribosylation-Factor-Like 2 Binding Protein, Cause Autosomal-Recessive Retinitis Pigmentosa. AMERICAN JOURNAL OF HUMAN GENETICS , 93 (2) pp. 321-329. 10.1016/j.ajhg.2013.06.003.

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Type: Article
Title: Mutations in ARL2BP, Encoding ADP-Ribosylation-Factor-Like 2 Binding Protein, Cause Autosomal-Recessive Retinitis Pigmentosa
DOI: 10.1016/j.ajhg.2013.06.003
Keywords: Science & Technology, Life Sciences & Biomedicine, Genetics & Heredity, PRIMARY CILIARY DYSKINESIA, BARDET-BIEDL-SYNDROME, PHOTORECEPTOR CELLS, PRIMARY CILIUM, PDE-DELTA, TRANSPORT, GENE, RP2, CILIOPATHIES, COMPLEX
UCL classification: UCL > Provost and Vice Provost Offices
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 Life Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Life Sciences > Div of Biosciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Life Sciences > Div of Biosciences > Genetics, Evolution and Environment
URI: http://discovery.ucl.ac.uk/id/eprint/1400173
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