Erratum: A dominant mutation in RPE65 identified by whole-exome sequencing causes retinitis pigmentosa with choroidal involvement (European Journal of Human Genetics (2011) 19 (1074-1081) DOI: 10.1038/ejhg.2011.86)

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 FarrarStephen P. Daiger, Peter Humphries

Research output: Contribution to journalArticle

Original languageEnglish
JournalEuropean Journal of Human Genetics
Volume19
Issue number10
DOIs
StatePublished - Oct 1 2011
Externally publishedYes

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Exome
Retinitis Pigmentosa
Medical Genetics
Mutation

ASJC Scopus subject areas

  • Genetics(clinical)
  • Genetics

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Erratum : A dominant mutation in RPE65 identified by whole-exome sequencing causes retinitis pigmentosa with choroidal involvement (European Journal of Human Genetics (2011) 19 (1074-1081) DOI: 10.1038/ejhg.2011.86). / Bowne, Sara J.; Humphries, Marian M.; Sullivan, Lori S.; Kenna, Paul F.; Tam, Lawrence C S; 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.

In: European Journal of Human Genetics, Vol. 19, No. 10, 01.10.2011.

Research output: Contribution to journalArticle

Bowne, SJ, Humphries, MM, Sullivan, LS, Kenna, PF, Tam, LCS, Kiang, AS, Campbell, M, Weinstock, GM, Koboldt, DC, Ding, L, Fulton, RS, Sodergren, EJ, Allman, D, Millington-Ward, S, Palfi, A, McKee, A, Blanton, SH, Slifer, S, Konidari, I, Farrar, GJ, Daiger, SP & Humphries, P 2011, 'Erratum: A dominant mutation in RPE65 identified by whole-exome sequencing causes retinitis pigmentosa with choroidal involvement (European Journal of Human Genetics (2011) 19 (1074-1081) DOI: 10.1038/ejhg.2011.86)', European Journal of Human Genetics, vol. 19, no. 10. https://doi.org/10.1038/ejhg.2011.132
Bowne, Sara J. ; Humphries, Marian M. ; Sullivan, Lori S. ; Kenna, Paul F. ; Tam, Lawrence C S ; 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. / Erratum : A dominant mutation in RPE65 identified by whole-exome sequencing causes retinitis pigmentosa with choroidal involvement (European Journal of Human Genetics (2011) 19 (1074-1081) DOI: 10.1038/ejhg.2011.86). In: European Journal of Human Genetics. 2011 ; Vol. 19, No. 10.
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