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Amendments and Corrections | 22 September 2011
Erratum: A dominant mutation in RPE65 identified by whole-exome sequencing causes retinitis pigmentosa with choroidal involvement
- Sara J Bowne
- , Marian M Humphries
- , Lori S Sullivan
- , Paul F Kenna
- , Lawrence CS Tam
- , Anna S Kiang
- , Matthew Campbell
- , George M Weinstock
- , Daniel C Koboldt
- , Li Ding
- , Robert S Fulton
- , Erica J Sodergren
- , Denis Allman
- , Sophia Millington-Ward
- , Arpad Palfi
- , Alex McKee
- , Susan H Blanton
- , Susan Slifer
- , Ioanna Konidari
- , G Jane Farrar
- , Stephen P Daiger
- & Peter Humphries
European Journal of Human Genetics 19 , 1109–1109

Rights & permissionsfor article Erratum: A dominant mutation in RPE65 identified by whole-exome sequencing causes retinitis pigmentosa with choroidal involvement . Opens in a new window.
7 July 2004
RNAi of COL1A1 in mesenchymal progenitor cells
- Sophia Millington-Ward
- , Helena P McMahon
- , Danny Allen
- , Gearóid Tuohy
- , Anna-Sophia Kiang
- , Arpad Palfi
- , Paul F Kenna
- , Peter Humphries
- & G Jane Farrar
European Journal of Human Genetics 12 , 864–866

Rights & permissionsfor article RNAi of COL1A1 in mesenchymal progenitor cells . Opens in a new window.
Research | 16 August 2016 | Open
microRNA regulatory circuits in a mouse model of inherited retinal degeneration
Scientific Reports 6 , 1–14

Rights & permissionsfor article microRNA regulatory circuits in a mouse model of inherited retinal degeneration . Opens in a new window.
Research | 6 June 2012 | Open
Intravitreal delivery of AAV-NDI1 provides functional benefit in a murine model of Leber hereditary optic neuropathy
- Naomi Chadderton
- , Arpad Palfi
- , Sophia Millington-Ward
- , Oliverio Gobbo
- , Nora Overlack
- , Matthew Carrigan
- , Mary O'Reilly
- , Matthew Campbell
- , Carsten Ehrhardt
- , Uwe Wolfrum
- , Peter Humphries
- , Paul F Kenna
- & G Jane Farrar
European Journal of Human Genetics 21 , 62–68

Rights & permissionsfor article Intravitreal delivery of AAV-NDI1 provides functional benefit in a murine model of Leber hereditary optic neuropathy . Opens in a new window.
Research | 8 June 2011
A dominant mutation in RPE65 identified by whole-exome sequencing causes retinitis pigmentosa with choroidal involvement
- Sara J Bowne
- , Marian M Humphries
- , Lori S Sullivan
- , Paul F Kenna
- , Lawrence C S Tam
- , Anna S Kiang
- , Matthew Campbell
- , George M Weinstock
- , Daniel C Koboldt
- , Li Ding
- , Robert S Fulton
- , Erica J Sodergren
- , Denis Allman
- , Sophia Millington-Ward
- , Arpad Palfi
- , Alex McKee
- , Susan H Blanton
- , Susan Slifer
- , Ioanna Konidari
- , G Jane Farrar
- , Stephen P Daiger
- & Peter Humphries
European Journal of Human Genetics 19 , 1074–1081

Rights & permissionsfor article A dominant mutation in RPE65 identified by whole-exome sequencing causes retinitis pigmentosa with choroidal involvement . Opens in a new window.

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Erratum: A dominant mutation in RPE65 identified by whole-exome sequencing causes retinitis pigmentosa with choroidal involvement

RNAi of COL1A1 in mesenchymal progenitor cells

microRNA regulatory circuits in a mouse model of inherited retinal degeneration

Intravitreal delivery of AAV-NDI1 provides functional benefit in a murine model of Leber hereditary optic neuropathy

A dominant mutation in RPE65 identified by whole-exome sequencing causes retinitis pigmentosa with choroidal involvement

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