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 Farrar; Stephen P. Daiger; Peter Humphries

doi:10.1038/ejhg.2011.132

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 journal › Comment/debate › peer-review

Original language	English (US)
Pages (from-to)	1109
Number of pages	1
Journal	European Journal of Human Genetics
Volume	19
Issue number	10
DOIs	https://doi.org/10.1038/ejhg.2011.132
State	Published - Oct 2011
Externally published	Yes

ASJC Scopus subject areas

Genetics
Genetics(clinical)

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10.1038/ejhg.2011.132

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Bowne, S. J., Humphries, M. M., Sullivan, L. S., Kenna, P. F., Tam, L. C. S., Kiang, A. S., Campbell, M., Weinstock, G. M., Koboldt, D. C., Ding, L., Fulton, R. S., Sodergren, E. J., Allman, D., Millington-Ward, S., Palfi, A., McKee, A., Blanton, S. H., Slifer, S., Konidari, I., ... 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, 19(10), 1109. https://doi.org/10.1038/ejhg.2011.132

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, 10.2011, p. 1109.

Research output: Contribution to journal › Comment/debate › peer-review

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, pp. 1109. https://doi.org/10.1038/ejhg.2011.132

Bowne SJ, Humphries MM, Sullivan LS, Kenna PF, Tam LCS, Kiang AS et al. 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. 2011 Oct;19(10):1109. 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. pp. 1109.

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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)

ASJC Scopus subject areas

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