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Published in Journal of neurochemistry (01.02.2010)
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Published in European journal of human genetics : EJHG (01.10.2011)
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Therapeutic benefit derived from RNAi-mediated ablation of IMPDH1 transcripts in a murine model of autosomal dominant retinitis pigmentosa (RP10)
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Published in Human molecular genetics (15.07.2008)
Published in Human molecular genetics (15.07.2008)
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Identification of an IMPDH1 mutation in autosomal dominant retinitis pigmentosa (RP10) revealed following comparative microarray analysis of transcripts derived from retinas of wild-type and Rho-/- mice
KENNAN, Avril, AHERNE, Aileen, KENNA, Paul F, FARRAR, G. Jane, HUMPHRIES, Pete, PALFI, Arpad, HUMPHRIES, Marian, MCKEE, Alex, STITT, Alan, SIMPSON, David A. C, DEMTRODER, Karin, ORNTOFT, Torben, AYUSO, Carmen
Published in Human molecular genetics (01.03.2002)
Published in Human molecular genetics (01.03.2002)
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Biofeedback in Heart Failure Patients Awaiting Transplantation
Frank, Dana, Baumann, Matthew, Khorshid, Lamees, PsyD, Liebenstein, Michael, PhD, Grossman-McKee, Alex, Kiffer, Jerome, McKee, Michael, Moravec, Christine
Published in Applied psychophysiology and biofeedback (01.09.2011)
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Published in Applied psychophysiology and biofeedback (01.09.2011)
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Erratum: A dominant mutation in RPE65 identified by whole-exome sequencing causes retinitis pigmentosa with choroidal involvement
Bowne, Sara J, Humphries, Marian M, Sullivan, Lori S, Kenna, Paul F, Tam, Lawrence CS, Kiang, Anna S, Campbell, Matthew, Weinstock, George M, Koboldt, Daniel C, Ding, Li, Fulton, Robert S, Sodergren, Erica J, Allman, Denis, Millington-Ward, Sophia, Palfi, Arpad, McKee, Alex, Blanton, Susan H, Slifer, Susan, Konidari, Ioanna, Farrar, G Jane, Daiger, Stephen P, Humphries, Peter
Published in European journal of human genetics : EJHG (22.09.2011)
Published in European journal of human genetics : EJHG (22.09.2011)
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Journal Article
A dominant mutation in RPE65 identified by whole-exome sequencing causes retinitis pigmentosa with choroidal involvement
Bowne, Sara J, Humphries, Marian M, Sullivan, Lori S, Kenna, Paul F, Tam, Lawrence Cs, Kiang, Anna S, Campbell, Matthew, Weinstock, George M, Koboldt, Daniel C, Ding, Li, Fulton, Robert S, Sodergren, Erica J, Allman, Denis, Millington-ward, Sophia, Palfi, Arpad, Mckee, Alex, Blanton, Susan H, Slifer, Susan, Konidari, Ioanna, Farrar, G Jane, Daiger, Stephen P, Humphries, Peter
Published in European journal of human genetics : EJHG (01.10.2011)
Published in European journal of human genetics : EJHG (01.10.2011)
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